Cleared Traditional

K863872 - TAMPER HAMPER
(FDA 510(k) Clearance)

K863872 · Hydro-Med Products, Inc. · General Hospital

Feb 1987

Decision

130d

Days

—

Risk

K863872 is an FDA 510(k) clearance for the TAMPER HAMPER. This device is classified as a Container, Frozen Donor Tissue Storage.

Submitted by Hydro-Med Products, Inc. (Dallas, US). The FDA issued a Cleared decision on February 10, 1987, 130 days after receiving the submission on October 3, 1986.

This device falls under the General Hospital FDA review panel.

Submission Details

510(k) Number	K863872 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	October 03, 1986
Decision Date	February 10, 1987
Days to Decision	130 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	—