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FDA 510(k)

DERMASEAL

K-Number: K960847 · 1996-04-04

ApplicantBellingham Medical, Inc.
Decision Date1996-04-04
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

DERMASEAL is the device name listed in this FDA 510(k) record. The listed applicant is Bellingham Medical, Inc.. It received FDA 510(k) clearance on 1996-04-04 under 510(k) number K960847. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMASEAL?

DERMASEAL is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Bellingham Medical, Inc.. The 510(k) number is K960847.

When did DERMASEAL receive FDA 510(k) clearance?

DERMASEAL received FDA 510(k) clearance on 1996-04-04, under 510(k) number K960847.

Who is the listed applicant for DERMASEAL?

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

What is the FDA product code for DERMASEAL?

The FDA product code for DERMASEAL is MGP.

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Related Devices (Code: MGP)

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.

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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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