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FDA 510(k)

HEMOVAC TUBING MATERIAL CHANGE

K-Number: K781400 · 1978-09-20

ApplicantSnyder Laboratories, Inc.
Decision Date1978-09-20
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEMOVAC TUBING MATERIAL CHANGE 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 1978-09-20 under 510(k) number K781400. 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 HEMOVAC TUBING MATERIAL CHANGE?

HEMOVAC TUBING MATERIAL CHANGE is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K781400.

When did HEMOVAC TUBING MATERIAL CHANGE receive FDA 510(k) clearance?

HEMOVAC TUBING MATERIAL CHANGE received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781400.

Who is the listed applicant for HEMOVAC TUBING MATERIAL CHANGE?

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 HEMOVAC TUBING MATERIAL CHANGE?

The FDA product code for HEMOVAC TUBING MATERIAL CHANGE 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 SOLUTIONK800543SNYDER HYSTERECTOMY Y TUBE KITK800577SNYDER HEMOVAC TM VENTED WOUND KITK800578SURGIVAC TM

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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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