510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810304Substantially Equivalent

Model Lc-85 UV Detector

Revvity Health Sciences, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810304 is the FDA 510(k) clearance record for MODEL LC-85 UV DETECTOR, a class I device, cleared for The Perkin-Elmer Corp. on under FDA product code LDM (Instrumentation, High Pressure Liquid Chromatography). FDA records list 81 510(k) clearances for Revvity Health Sciences, Inc., from to . As of , FDA records show no recalls naming K810304.

Clearance record

Decision date
Received
(20 days to decision)
Product code
LDM Instrumentation, High Pressure Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Applicant
The Perkin-Elmer Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LDM

Trailing 12 months

FDA records hold no clearances under product code LDM in the trailing twelve months.

FDA records show no clearances under product code LDM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260