510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771919Substantially Equivalent

Fiber Optics Sigmoidoscope

Propper Mfg Co Inc, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771919 is the FDA 510(k) clearance record for FIBER OPTICS SIGMOIDOSCOPE, a class II device, cleared for Propper Mfg. Co., Inc. on under FDA product code GCP (Endoscope, Ac-Powered And Accessories). FDA records list 25 510(k) clearances for Propper Mfg. Co., Inc., from to . As of , FDA records show no recalls naming K771919.

Clearance record

Decision date
Received
(8 days to decision)
Product code
GCP Endoscope, Ac-Powered And Accessories
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Propper Mfg. Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GCP

Trailing 12 months

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

FDA records show no clearances under product code GCP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GCP, 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