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FDA 510(k)

TEST KIT, IIF-ANA

K-Number: K782048 · 1979-01-17

ApplicantMedica Corp.
Decision Date1979-01-17
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TEST KIT, IIF-ANA is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K782048. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST KIT, IIF-ANA?

TEST KIT, IIF-ANA is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Medica Corp.. The 510(k) number is K782048.

When did TEST KIT, IIF-ANA receive FDA 510(k) clearance?

TEST KIT, IIF-ANA received FDA 510(k) clearance on 1979-01-17, under 510(k) number K782048.

Who is the listed applicant for TEST KIT, IIF-ANA?

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

What is the FDA product code for TEST KIT, IIF-ANA?

The FDA product code for TEST KIT, IIF-ANA is DHN.

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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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