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FDA 510(k)

CATH KIT, SUPERPUBIC

K-Number: K772227 · 1977-12-20

Decision Date1977-12-20
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATH KIT, SUPERPUBIC is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772227. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH KIT, SUPERPUBIC?

CATH KIT, SUPERPUBIC is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K772227.

When did CATH KIT, SUPERPUBIC receive FDA 510(k) clearance?

CATH KIT, SUPERPUBIC received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772227.

Who is the listed applicant for CATH KIT, SUPERPUBIC?

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

What is the FDA product code for CATH KIT, SUPERPUBIC?

The FDA product code for CATH KIT, SUPERPUBIC is KXF.

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 Hospital Supply 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 56 devices →

Related Devices (Code: KXF)

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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