SNYDER HEMOVAC WOUND DRAINAGE DEVICES— 510(k) K843906

Name: FDA 510(k) clearance K843906
Creator: U.S. Food and Drug Administration
Published: 1984-11-05

Substantially Equivalent

Snyder Laboratories, Inc.

FDA 510(k) clearance K843906 for SNYDER HEMOVAC WOUND DRAINAGE DEVICES, Substantially Equivalent on 1984-11-05. Applicant: Snyder Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Snyder Laboratories, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1984-10-03
Decision date: 1984-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Philadelphia, OH, US

Download summary PDF View on FDA.gov ↗

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K880376 — NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP1988-02-16

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K800543 — SNYDER HYSTERECTOMY Y TUBE KIT1980-04-16
K800577 — SNYDER HEMOVAC TM VENTED WOUND KIT1980-04-16
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