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FDA 510(k)

ARTERIAL MICROCOLLECTION SET

K-Number: K810308 · 1981-02-19

ApplicantAmerican Dade
Decision Date1981-02-19
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ARTERIAL MICROCOLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is American Dade. It received FDA 510(k) clearance on 1981-02-19 under 510(k) number K810308. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL MICROCOLLECTION SET?

ARTERIAL MICROCOLLECTION SET is a medical device that received FDA 510(k) clearance on 1981-02-19. The listed applicant is American Dade. The 510(k) number is K810308.

When did ARTERIAL MICROCOLLECTION SET receive FDA 510(k) clearance?

ARTERIAL MICROCOLLECTION SET received FDA 510(k) clearance on 1981-02-19, under 510(k) number K810308.

Who is the listed applicant for ARTERIAL MICROCOLLECTION SET?

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

What is the FDA product code for ARTERIAL MICROCOLLECTION SET?

The FDA product code for ARTERIAL MICROCOLLECTION SET is CHL.

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Other records listing American Dade as applicant

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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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