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FDA 510(k)

POROUS, BREATHING TAPE W/RELEASE LINER

K-Number: K802752 · 1980-12-10

Decision Date1980-12-10
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POROUS, BREATHING TAPE W/RELEASE LINER is the device name listed in this FDA 510(k) record. The listed applicant is Bioadhesive Systems, Inc.. It received FDA 510(k) clearance on 1980-12-10 under 510(k) number K802752. 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 POROUS, BREATHING TAPE W/RELEASE LINER?

POROUS, BREATHING TAPE W/RELEASE LINER is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Bioadhesive Systems, Inc.. The 510(k) number is K802752.

When did POROUS, BREATHING TAPE W/RELEASE LINER receive FDA 510(k) clearance?

POROUS, BREATHING TAPE W/RELEASE LINER received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802752.

Who is the listed applicant for POROUS, BREATHING TAPE W/RELEASE LINER?

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

What is the FDA product code for POROUS, BREATHING TAPE W/RELEASE LINER?

The FDA product code for POROUS, BREATHING TAPE W/RELEASE LINER is KGX.

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.

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.

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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