510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K901937Substantially Equivalent

Codman Suction Pattie

Cerenovus, Inc., Randolph MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901937 is the FDA 510(k) clearance record for CODMAN SUCTION PATTIE, a class II device, cleared for Codman & Shurtleff, Inc. on under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered). FDA records list 163 510(k) clearances for Cerenovus, Inc., from to . As of , FDA records show no recalls naming K901937.

Clearance record

Decision date
Received
(77 days to decision)
Product code
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Codman & Shurtleff, Inc. 41 Pacella Park Dr., Randolph MA
Third party review
No

Clearances, product code GCX

Trailing 12 months

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

FDA records show no clearances under product code GCX in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GCX, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260