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FDA 510(k)

MEDIMAC BANDAGE

K-Number: K930457 · 1994-01-25

ApplicantEnquay Pharmaceutical
Decision Date1994-01-25
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDIMAC BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Enquay Pharmaceutical. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K930457. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIMAC BANDAGE?

MEDIMAC BANDAGE is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Enquay Pharmaceutical. The 510(k) number is K930457.

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

MEDIMAC BANDAGE received FDA 510(k) clearance on 1994-01-25, under 510(k) number K930457.

Who is the listed applicant for MEDIMAC BANDAGE?

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

What is the FDA product code for MEDIMAC BANDAGE?

The FDA product code for MEDIMAC BANDAGE is KGX.

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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