FDA 510(k)

PRO-TAB

K-Number: K790547 · 1979-04-03

Decision Date1979-04-03

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PRO-TAB is the device name listed in this FDA 510(k) record. The listed applicant is Professional Tape Co., Inc.. It received FDA 510(k) clearance on 1979-04-03 under 510(k) number K790547. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TAB?

PRO-TAB is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Professional Tape Co., Inc.. The 510(k) number is K790547.

When did PRO-TAB receive FDA 510(k) clearance?

PRO-TAB received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790547.

Who is the listed applicant for PRO-TAB?

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

What is the FDA product code for PRO-TAB?

The FDA product code for PRO-TAB is KCT.

Other records listing Professional Tape Co., Inc. 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.

K800873TIME STEAM AUTOCLAVE TAPE

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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.