510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K843906Substantially Equivalent

Snyder Hemovac Wound Drainage Devices

Snyder Laboratories, Inc., New Philadelphia OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843906 is the FDA 510(k) clearance record for SNYDER HEMOVAC WOUND DRAINAGE DEVICES, a class I device, cleared for Snyder Laboratories, Inc. on under FDA product code GBS (Catheter, Ventricular, General & Plastic Surgery). FDA records list 16 510(k) clearances for Snyder Laboratories, Inc., from to . As of , FDA records show no recalls naming K843906.

Clearance record

Decision date
Received
(33 days to decision)
Product code
GBS Catheter, Ventricular, General & Plastic Surgery
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Snyder Laboratories, Inc. P.O. Box 409, New Philadelphia OH
Third party review
No

Clearances, product code GBS

Trailing 12 months

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

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