K872737Substantially Equivalent

Perkin-Elmer Lc235 Diode Array Detector

Name: K872737 Perkin-Elmer Lc235 Diode Array Detector
Creator: The Perkin-Elmer Corp.
Published: 1987-09-18
License: https://open.fda.gov/license/

Revvity Health Sciences, Inc., CT / Traditional, Substantially Equivalent

FDA source

K872737 is the FDA 510(k) clearance record for PERKIN-ELMER LC235 DIODE ARRAY DETECTOR, cleared for The Perkin-Elmer Corp. on 1987-09-18. FDA records list 81 510(k) clearances for Revvity Health Sciences, Inc., from 1976-07-16 to 2022-11-09. As of 2026-09-10, FDA records show no recalls naming K872737.

Clearance record

Decision date: 1987-09-18
Received: 1987-07-09 (71 days to decision)
Review panel: Unknown
Applicant: The Perkin-Elmer Corp.
Third party review: No