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FDA 510(k)

SURGIVAC TM

K-Number: K800578 · 1980-04-16

ApplicantSnyder Laboratories, Inc.
Decision Date1980-04-16
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGIVAC TM 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 1980-04-16 under 510(k) number K800578. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGIVAC TM?

SURGIVAC TM is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K800578.

When did SURGIVAC TM receive FDA 510(k) clearance?

SURGIVAC TM received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800578.

Who is the listed applicant for SURGIVAC TM?

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 SURGIVAC TM?

The FDA product code for SURGIVAC TM is GCY.

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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.

K843906SNYDER HEMOVAC WOUND DRAINAGE DEVICESK821321SNYDER DEBRIBEMENT SYSTEM LDP-1K800861SNYDER HEMOVAC CHEST DRAINAGE SOLUTIONK800577SNYDER HEMOVAC TM VENTED WOUND KITK800543SNYDER HYSTERECTOMY Y TUBE KITK800542100 ML SNYDER HEMOVAC

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Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, 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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