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FDA 510(k)

MICROFLEX-VENOFLUX

K-Number: K822836 · 1982-10-15

ApplicantExco, Inc.
Decision Date1982-10-15
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROFLEX-VENOFLUX is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1982-10-15 under 510(k) number K822836. 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 MICROFLEX-VENOFLUX?

MICROFLEX-VENOFLUX is a medical device that received FDA 510(k) clearance on 1982-10-15. The listed applicant is Exco, Inc.. The 510(k) number is K822836.

When did MICROFLEX-VENOFLUX receive FDA 510(k) clearance?

MICROFLEX-VENOFLUX received FDA 510(k) clearance on 1982-10-15, under 510(k) number K822836.

Who is the listed applicant for MICROFLEX-VENOFLUX?

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

What is the FDA product code for MICROFLEX-VENOFLUX?

The FDA product code for MICROFLEX-VENOFLUX is FPA.

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Other records listing Exco, Inc. as applicant

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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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