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FDA 510(k)

DERMCO A-I

K-Number: K923400 · 1992-10-06

ApplicantDermaco, Inc.
Decision Date1992-10-06
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMCO A-I is the device name listed in this FDA 510(k) record. The listed applicant is Dermaco, Inc.. It received FDA 510(k) clearance on 1992-10-06 under 510(k) number K923400. 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 DERMCO A-I?

DERMCO A-I is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Dermaco, Inc.. The 510(k) number is K923400.

When did DERMCO A-I receive FDA 510(k) clearance?

DERMCO A-I received FDA 510(k) clearance on 1992-10-06, under 510(k) number K923400.

Who is the listed applicant for DERMCO A-I?

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

What is the FDA product code for DERMCO A-I?

The FDA product code for DERMCO A-I 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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