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FDA 510(k)

HYPO-ALLERGENIC PLASTIC TAPE

K-Number: K792136 · 1980-01-16

Decision Date1980-01-16
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPO-ALLERGENIC PLASTIC TAPE is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792136. 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 HYPO-ALLERGENIC PLASTIC TAPE?

HYPO-ALLERGENIC PLASTIC TAPE is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is National Patent Development Corp.. The 510(k) number is K792136.

When did HYPO-ALLERGENIC PLASTIC TAPE receive FDA 510(k) clearance?

HYPO-ALLERGENIC PLASTIC TAPE received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792136.

Who is the listed applicant for HYPO-ALLERGENIC PLASTIC TAPE?

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

What is the FDA product code for HYPO-ALLERGENIC PLASTIC TAPE?

The FDA product code for HYPO-ALLERGENIC PLASTIC TAPE 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 National Patent Development 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.

View all 34 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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