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FDA 510(k)

VENIPUNCTURE VALVE

K-Number: K832123 · 1983-08-12

ApplicantAbbott Laboratories
Decision Date1983-08-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENIPUNCTURE VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832123. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENIPUNCTURE VALVE?

VENIPUNCTURE VALVE is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Abbott Laboratories. The 510(k) number is K832123.

When did VENIPUNCTURE VALVE receive FDA 510(k) clearance?

VENIPUNCTURE VALVE received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832123.

Who is the listed applicant for VENIPUNCTURE VALVE?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENIPUNCTURE VALVE?

The FDA product code for VENIPUNCTURE VALVE is FPA.

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Related Devices (Code: FPA)

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.

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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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