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FDA 510(k)

SKIN CLOSURE TAPES STERILE

K-Number: K790140 · 1979-02-27

Decision Date1979-02-27
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIN CLOSURE TAPES STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Shur Medical Corp.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790140. 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 SKIN CLOSURE TAPES STERILE?

SKIN CLOSURE TAPES STERILE is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Shur Medical Corp.. The 510(k) number is K790140.

When did SKIN CLOSURE TAPES STERILE receive FDA 510(k) clearance?

SKIN CLOSURE TAPES STERILE received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790140.

Who is the listed applicant for SKIN CLOSURE TAPES STERILE?

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

What is the FDA product code for SKIN CLOSURE TAPES STERILE?

The FDA product code for SKIN CLOSURE TAPES STERILE 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 Shur Medical Corp. 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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