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FDA 510(k)

MEDICA II-F-ASMA TEST KIT

K-Number: K790430 · 1979-04-23

ApplicantMedica Corp.
Decision Date1979-04-23
Product CodeDBE
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

MEDICA II-F-ASMA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790430. The device is classified under product code DBE. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICA II-F-ASMA TEST KIT?

MEDICA II-F-ASMA TEST KIT is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Medica Corp.. The 510(k) number is K790430.

When did MEDICA II-F-ASMA TEST KIT receive FDA 510(k) clearance?

MEDICA II-F-ASMA TEST KIT received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790430.

Who is the listed applicant for MEDICA II-F-ASMA TEST KIT?

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 MEDICA II-F-ASMA TEST KIT?

The FDA product code for MEDICA II-F-ASMA TEST KIT is DBE.

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Other records listing Medica Corp. as applicant

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Related Devices (Code: DBE)

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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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