Cleared Traditional

PERKIN-ELMER LC235 DIODE ARRAY DETECTOR

K872737 · The Perkin-Elmer Corp. · Toxicology

Sep 1987

Decision

71d

Days

—

Risk

About This 510(k) Submission

K872737 is an FDA 510(k) clearance for the PERKIN-ELMER LC235 DIODE ARRAY DETECTOR, submitted by The Perkin-Elmer Corp.. The FDA issued a Cleared decision on September 18, 1987, 71 days after receiving the submission on July 9, 1987. This device falls under the Toxicology review panel.

Submission Details

510(k) Number	K872737 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 09, 1987
Decision Date	September 18, 1987
Days to Decision	71 days
Submission Type	Traditional
Review Panel	Toxicology (TX)
Summary	—