510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K061651Substantially Equivalent

Fischer Cone Biopsy Excisor, Models 900-150, 151, 152, 154, 155, 157 and 158

CooperSurgical, Inc., Marlboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K061651 is the FDA 510(k) clearance record for FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158, a class II device, cleared for Apple Medical Corp. on under FDA product code HGI (Electrocautery, Gynecologic (And Accessories)). FDA records list 103 510(k) clearances for COOPERSURGICAL, INC., from to . As of , FDA records show 2 recalls naming K061651.

Clearance record

Decision date
Received
(129 days to decision)
Product code
HGI Electrocautery, Gynecologic (And Accessories)
Regulation
21 CFR 884.4120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Apple Medical Corp. 28 Lord Rd., Unit 135, Marlboro MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HGI

Trailing 12 months

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

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