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FDA 510(k)

LATEX PENROSE DRAIN TUBING

K-Number: K821700 · 1982-06-16

ApplicantAbco Dealers, Inc.
Decision Date1982-06-16
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LATEX PENROSE DRAIN TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1982-06-16 under 510(k) number K821700. The device is classified under product code GAX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX PENROSE DRAIN TUBING?

LATEX PENROSE DRAIN TUBING is a medical device that received FDA 510(k) clearance on 1982-06-16. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K821700.

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

LATEX PENROSE DRAIN TUBING received FDA 510(k) clearance on 1982-06-16, under 510(k) number K821700.

Who is the listed applicant for LATEX PENROSE DRAIN TUBING?

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

What is the FDA product code for LATEX PENROSE DRAIN TUBING?

The FDA product code for LATEX PENROSE DRAIN TUBING is GAX.

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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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