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FDA 510(k)

GOODMAN BANDAGE

K-Number: K933085 · 1993-12-23

ApplicantMegadyne Medical Products, Inc.
Decision Date1993-12-23
Product CodeKGY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GOODMAN BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1993-12-23 under 510(k) number K933085. The device is classified under product code KGY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOODMAN BANDAGE?

GOODMAN BANDAGE is a medical device that received FDA 510(k) clearance on 1993-12-23. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K933085.

When did GOODMAN BANDAGE receive FDA 510(k) clearance?

GOODMAN BANDAGE received FDA 510(k) clearance on 1993-12-23, under 510(k) number K933085.

Who is the listed applicant for GOODMAN BANDAGE?

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

What is the FDA product code for GOODMAN BANDAGE?

The FDA product code for GOODMAN BANDAGE is KGY.

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Other records listing Megadyne Medical Products, 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.

K233644Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)K213696ETHICON Megadyne Electrosurgical GeneratorK200250Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF SensorK193145Ethicon Megadyne Electrosurgical Generator, Bipolar FootswitchK191328Megadyne Foot SwitchK080741MEGA SOFT REUSABLE PATIENT RETURN ELECTRODE

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Related Devices (Code: KGY)

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.

K913678TROCAR CATHETERMedovations, Inc.K910914SURGICAL TISSUE POUCHCook Urological, Inc.K832318ISOLATION BAG 3M3M CompanyK801824BAND-AID BRAND FLEXIBLE FABRIC BANDAGEJohnson & Johnson Professionals, Inc.K801823BAND-AID BRAND TRICOT MESH BANDAGESJohnson & Johnson Professionals, 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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