Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LATEX PENROSE TUBING CAT. #20400,414,416

K-Number: K802761 · 1980-11-19

Decision Date1980-11-19
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX PENROSE TUBING CAT. #20400,414,416 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 1980-11-19 under 510(k) number K802761. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX PENROSE TUBING CAT. #20400,414,416?

LATEX PENROSE TUBING CAT. #20400,414,416 is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K802761.

When did LATEX PENROSE TUBING CAT. #20400,414,416 receive FDA 510(k) clearance?

LATEX PENROSE TUBING CAT. #20400,414,416 received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802761.

Who is the listed applicant for LATEX PENROSE TUBING CAT. #20400,414,416?

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 LATEX PENROSE TUBING CAT. #20400,414,416?

The FDA product code for LATEX PENROSE TUBING CAT. #20400,414,416 is GAZ.

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: GAZ)

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.

↑