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FDA 510(k)

ANDOVER MOLESKIN

K-Number: K872594 · 1987-08-04

ApplicantAndover Coated Products, Inc.
Decision Date1987-08-04
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANDOVER MOLESKIN is the device name listed in this FDA 510(k) record. The listed applicant is Andover Coated Products, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872594. 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 ANDOVER MOLESKIN?

ANDOVER MOLESKIN is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Andover Coated Products, Inc.. The 510(k) number is K872594.

When did ANDOVER MOLESKIN receive FDA 510(k) clearance?

ANDOVER MOLESKIN received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872594.

Who is the listed applicant for ANDOVER MOLESKIN?

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

What is the FDA product code for ANDOVER MOLESKIN?

The FDA product code for ANDOVER MOLESKIN is KGX.

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Other records listing Andover Coated 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.

K872593ANDOVER ADHESIVE TAPE, SURGICAL

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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