510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K130282Substantially Equivalent

Remington Medical Centrefire 22 Biopsy Instrument

Remington Medical, Alpharetta GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130282 is the FDA 510(k) clearance record for REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT, a class II device, cleared for Remington Medical, Inc. on under FDA product code KNW (Instrument, Biopsy). FDA records list 19 510(k) clearances for Remington Medical, Inc., from to . As of , FDA records show no recalls naming K130282.

Clearance record

Decision date
Received
(97 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Remington Medical, Inc. 6830 Meadowridge Ct., Alpharetta GA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code KNW

Trailing 12 months
8 clearances under product code KNW in the twelve months to October 2026, August 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code KNW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20260
August 20264
September 20260
October 20260