510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K922971Substantially Equivalent

No-Scalpel Vascetomy Instruments

Pilling Co., Fort Washington PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922971 is the FDA 510(k) clearance record for NO-SCALPEL VASCETOMY INSTRUMENTS, a class I device, cleared for Pilling Co. on under FDA product code KOA (Surgical Instruments, G-U, Manual (And Accessories)). FDA records list 40 510(k) clearances for Pilling Co., from to . As of , FDA records show no recalls naming K922971.

Clearance record

Decision date
Received
(96 days to decision)
Product code
KOA Surgical Instruments, G-U, Manual (And Accessories)
Regulation
21 CFR 876.4730
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Pilling Co. 420 Delaware Dr., Fort Washington PA
510(k) summary
Statement
Third party review
No

Clearances, product code KOA

Trailing 12 months

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

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