FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SNYDER HEMOVAC WOUND DRAINAGE DEVICES

K Number: K843906 · Decision Nov 5, 1984
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
16
Review Days
33

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Basic Information

Device Name
SNYDER HEMOVAC WOUND DRAINAGE DEVICES
K Number
K843906
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Snyder Laboratories, Inc.
Date Received
October 3, 1984
Decision Date
November 5, 1984
Product Code
GBS
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GBS Catheter, Ventricular, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBS), ordered by most recent decision date.

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Other Clearances by Snyder Laboratories, Inc.

K Number Device Name
K821321 SNYDER DEBRIBEMENT SYSTEM LDP-1
K800861 SNYDER HEMOVAC CHEST DRAINAGE SOLUTION
K800543 SNYDER HYSTERECTOMY Y TUBE KIT
K800577 SNYDER HEMOVAC TM VENTED WOUND KIT
K800578 SURGIVAC TM
K800542 100 ML SNYDER HEMOVAC
K790607 GREENLINE IRRIGATION TRAYS
K790606 CATHETERS, GREENLINE SUCTION
K790420 SUCTION CONNECTING TUBING
K790419 YANKAUER & POODLE SUCTION INSTRUMENTS
Search all 16 clearances from Snyder Laboratories, Inc. →