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FDA 510(k)

SNYDER HEMOVAC WOUND DRAINAGE DEVICES

K-Number: K843906 · 1984-11-05

ApplicantSnyder Laboratories, Inc.
Decision Date1984-11-05
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SNYDER HEMOVAC WOUND DRAINAGE DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Laboratories, Inc.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K843906. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNYDER HEMOVAC WOUND DRAINAGE DEVICES?

SNYDER HEMOVAC WOUND DRAINAGE DEVICES is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K843906.

When did SNYDER HEMOVAC WOUND DRAINAGE DEVICES receive FDA 510(k) clearance?

SNYDER HEMOVAC WOUND DRAINAGE DEVICES received FDA 510(k) clearance on 1984-11-05, under 510(k) number K843906.

Who is the listed applicant for SNYDER HEMOVAC WOUND DRAINAGE DEVICES?

The FDA 510(k) record lists Snyder Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNYDER HEMOVAC WOUND DRAINAGE DEVICES?

The FDA product code for SNYDER HEMOVAC WOUND DRAINAGE DEVICES is GBS.

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Other records listing Snyder Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K821321SNYDER DEBRIBEMENT SYSTEM LDP-1K800861SNYDER HEMOVAC CHEST DRAINAGE SOLUTIONK800543SNYDER HYSTERECTOMY Y TUBE KITK800577SNYDER HEMOVAC TM VENTED WOUND KITK800578SURGIVAC TMK800542100 ML SNYDER HEMOVAC

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Related Devices (Code: GBS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K912645ATRIUMS PDR THORACIC CATHETERAtrium Medical Corp.K883887AXIOM ATRAUM WOUND DRAINSAxiom, Inc.K881873INTRODUCTION/DRAINAGE CATHETER & ACCESSSheridan Catheter Corp.K880895URESIL WOUND DRAIN TROCARUresil Corp.K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPGenesis Industries, Inc.K873377CLOSED CHEST DRAINAGE SET W/SUTURESGish Biomedical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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