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FDA 510(k)

SURGITEK FOERSTER FACE LIFT DRAIN

K-Number: K800331 · 1980-03-05

ApplicantMedical Engineering Corp.
Decision Date1980-03-05
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGITEK FOERSTER FACE LIFT DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Corp.. It received FDA 510(k) clearance on 1980-03-05 under 510(k) number K800331. 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 SURGITEK FOERSTER FACE LIFT DRAIN?

SURGITEK FOERSTER FACE LIFT DRAIN is a medical device that received FDA 510(k) clearance on 1980-03-05. The listed applicant is Medical Engineering Corp.. The 510(k) number is K800331.

When did SURGITEK FOERSTER FACE LIFT DRAIN receive FDA 510(k) clearance?

SURGITEK FOERSTER FACE LIFT DRAIN received FDA 510(k) clearance on 1980-03-05, under 510(k) number K800331.

Who is the listed applicant for SURGITEK FOERSTER FACE LIFT DRAIN?

The FDA 510(k) record lists Medical Engineering Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGITEK FOERSTER FACE LIFT DRAIN?

The FDA product code for SURGITEK FOERSTER FACE LIFT DRAIN is GCY.

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Other records listing Medical Engineering Corp. as applicant

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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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