Medical Device Manufacturer · US , Irvine , CA

Disease Detection International, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1988

Total

Cleared

Denied

Disease Detection International, Inc. has 20 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 20 cleared submissions from 1988 to 1994. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Disease Detection International, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Disease Detection International, Inc.

20 devices

1-12 of 20

Cleared Oct 25, 1994

PRO-STEP LH OVULATION PREDICTION TEST

IMMUNOCARD HCG ONE STEP (I-S) TEST KIT

K911826 · JHI

Chemistry · 86d

Cleared Sep 05, 1990

MODIFICATION OF SEROCARD RUBELLA IGG TEST

K902571 · LFX

Microbiology · 90d

Cleared Aug 09, 1990

SEROCARD HSV IGG ANTIBODY TEST KIT

K903070 · LGC

Microbiology · 28d

Cleared Dec 01, 1989

IMMUNOCARD HCG II-S TEST KIT

K895912 · JHI

Chemistry · 52d

Cleared Nov 29, 1989

IMMUNOCARD STREP A TEST

K896109 · GTZ

Microbiology · 37d

Cleared Apr 10, 1989

MODIFIED DDI SEROCARD HERPES IGG TEST KIT

K884246 · LGC

Microbiology · 181d

Cleared Apr 10, 1989

MODIFIED DDI SEROCARD RUBELLA IGG TEST KIT

K884247 · LFX

Microbiology · 181d

Cleared Apr 10, 1989

MODIFIED DDI SEROCARD CMV IGG TEST KIT

K884248 · LFZ

Microbiology · 181d

Cleared Apr 10, 1989

MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT

K884249 · LGD

Microbiology · 181d

Disease Detection International, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Disease Detection International, Inc.

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