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FDA 510(k)

LATEX PENROSE TUBING

K-Number: K822755 · 1983-01-21

ApplicantAmerican Hospital Supply Corp.
Decision Date1983-01-21
Product Code
DecisionSubstantially Equivalent

Device Summary

LATEX PENROSE TUBING 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 1983-01-21 under 510(k) number K822755. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX PENROSE TUBING?

LATEX PENROSE TUBING is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K822755.

When did LATEX PENROSE TUBING receive FDA 510(k) clearance?

LATEX PENROSE TUBING received FDA 510(k) clearance on 1983-01-21, under 510(k) number K822755.

Who is the listed applicant for LATEX PENROSE TUBING?

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

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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.

K854739AMERICAN STERILE SURGICAL ABSORBENT TOWELK854759AMERICAN STERILE MAYO STAND TRAYK832826AAP DOSIMETRY RELEASE OR BASIN SETSK830546DOSIMETRIC RELEASEK822990CONVERTORS PRIMARY WOUND DRESSING IIK830343CONTAINER W/PRIMING SOLUTION

View all 56 devices →

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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