510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980972Substantially Equivalent

Rigid Culdoscope and Accessories

Circon Corp., Santa Barbara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980972 is the FDA 510(k) clearance record for RIGID CULDOSCOPE AND ACCESSORIES, a class II device, cleared for Circon Corp. on under FDA product code HEW (Culdoscope (And Accessories)). FDA records list 6 510(k) clearances for Circon Corp., from to . As of , FDA records show no recalls naming K980972.

Clearance record

Decision date
Received
(88 days to decision)
Product code
HEW Culdoscope (And Accessories)
Regulation
21 CFR 884.1640
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Circon Corp. 6500 Hollister Ave., Santa Barbara CA
510(k) summary
Summary
Third party review
No

Clearances, product code HEW

Trailing 12 months

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

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