FDA 510(k)

BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER

K-Number: K971763 · 1997-08-26

Decision Date1997-08-26

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Retractable Technologies, Inc.. It received FDA 510(k) clearance on 1997-08-26 under 510(k) number K971763. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER?

BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER is a medical device that received FDA 510(k) clearance on 1997-08-26. The listed applicant is Retractable Technologies, Inc.. The 510(k) number is K971763.

When did BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER receive FDA 510(k) clearance?

BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER received FDA 510(k) clearance on 1997-08-26, under 510(k) number K971763.

Who is the listed applicant for BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER?

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

What is the FDA product code for BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER?

The FDA product code for BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER is FMI.

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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.