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FDA 510(k)

DERMA SEAL

K-Number: K952702 · 1995-06-28

ApplicantTtl Medical
Decision Date1995-06-28
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMA SEAL is the device name listed in this FDA 510(k) record. The listed applicant is Ttl Medical. It received FDA 510(k) clearance on 1995-06-28 under 510(k) number K952702. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMA SEAL?

DERMA SEAL is a medical device that received FDA 510(k) clearance on 1995-06-28. The listed applicant is Ttl Medical. The 510(k) number is K952702.

When did DERMA SEAL receive FDA 510(k) clearance?

DERMA SEAL received FDA 510(k) clearance on 1995-06-28, under 510(k) number K952702.

Who is the listed applicant for DERMA SEAL?

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

What is the FDA product code for DERMA SEAL?

The FDA product code for DERMA SEAL is FPX.

Related Clinical Trials

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.

Other records listing Ttl Medical 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.

Related Devices (Code: FPX)

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.

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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