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FDA 510(k)

REGULATOR VENOSET W/0.22 MICRON IVEX

K-Number: K810029 · 1981-01-06

ApplicantAbbott Laboratories
Decision Date1981-01-06
Product Code
DecisionUnknown

Device Summary

REGULATOR VENOSET W/0.22 MICRON IVEX is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1981-01-06 under 510(k) number K810029. FDA Decision: Unknown.

Frequently Asked Questions

What is the REGULATOR VENOSET W/0.22 MICRON IVEX?

REGULATOR VENOSET W/0.22 MICRON IVEX is a medical device that received FDA 510(k) clearance on 1981-01-06. The listed applicant is Abbott Laboratories. The 510(k) number is K810029.

When did REGULATOR VENOSET W/0.22 MICRON IVEX receive FDA 510(k) clearance?

REGULATOR VENOSET W/0.22 MICRON IVEX received FDA 510(k) clearance on 1981-01-06, under 510(k) number K810029.

Who is the listed applicant for REGULATOR VENOSET W/0.22 MICRON IVEX?

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

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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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