510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872867Substantially Equivalent

Biosign

Clinical Technology Inc., Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872867 is the FDA 510(k) clearance record for BIOSIGN, a class II device, cleared for Clinical Technology Corp. on under FDA product code FRC (Indicator, Biological Sterilization Process). FDA records list 12 510(k) clearances for Clinical Technology Corp., from to . As of , FDA records show no recalls naming K872867.

Clearance record

Decision date
Received
(351 days to decision)
Product code
FRC Indicator, Biological Sterilization Process
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Clinical Technology Corp. 3750 Monroe Ave., Rochester NY
Third party review
No

Clearances, product code FRC

Trailing 12 months
1 clearance under product code FRC in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FRC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260