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FDA 510(k)

TACKMER INCISE DRAPE

K-Number: K802050 · 1980-09-16

Decision Date1980-09-16
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TACKMER INCISE DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is American Convertors Div., American Pharmaseal. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K802050. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TACKMER INCISE DRAPE?

TACKMER INCISE DRAPE is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is American Convertors Div., American Pharmaseal. The 510(k) number is K802050.

When did TACKMER INCISE DRAPE receive FDA 510(k) clearance?

TACKMER INCISE DRAPE received FDA 510(k) clearance on 1980-09-16, under 510(k) number K802050.

Who is the listed applicant for TACKMER INCISE DRAPE?

The FDA 510(k) record lists American Convertors Div., American Pharmaseal as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TACKMER INCISE DRAPE?

The FDA product code for TACKMER INCISE DRAPE is KKX.

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 American Convertors Div., American Pharmaseal 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 19 devices →

Related Devices (Code: KKX)

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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