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FDA 510(k)

SALONMAY BUSTLINE INCREASER

K-Number: K770082 · 1977-03-16

ApplicantGamma Enterprises, Inc.
Decision Date1977-03-16
Product CodeMWZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SALONMAY BUSTLINE INCREASER is the device name listed in this FDA 510(k) record. The listed applicant is Gamma Enterprises, Inc.. It received FDA 510(k) clearance on 1977-03-16 under 510(k) number K770082. The device is classified under product code MWZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALONMAY BUSTLINE INCREASER?

SALONMAY BUSTLINE INCREASER is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Gamma Enterprises, Inc.. The 510(k) number is K770082.

When did SALONMAY BUSTLINE INCREASER receive FDA 510(k) clearance?

SALONMAY BUSTLINE INCREASER received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770082.

Who is the listed applicant for SALONMAY BUSTLINE INCREASER?

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

What is the FDA product code for SALONMAY BUSTLINE INCREASER?

The FDA product code for SALONMAY BUSTLINE INCREASER is MWZ.

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Other records listing Gamma Enterprises, 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.

K790578GAMMA SMAC REAGENTSK780507SERUM GLUTAMIC-PYRUVIC TRANSAMINASEK780506CARBON DIOXIDE REAGENTSK780505SERUM GLUTAMIC-OXALOACETIC-TRANSAMINASEK780504CREATINE PHOSPHOKINASE (CPK)K771836LACTATE DEHYDROGENASE

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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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