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FDA 510(k)

KALLESTAD FLORESCENT ANA/AMA/ASMA TEST

K-Number: K792610 · 1980-02-22

ApplicantKallestad Laboratories, Inc.
Decision Date1980-02-22
Product CodeDBL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

KALLESTAD FLORESCENT ANA/AMA/ASMA TEST is the device name listed in this FDA 510(k) record. The listed applicant is Kallestad Laboratories, Inc.. It received FDA 510(k) clearance on 1980-02-22 under 510(k) number K792610. The device is classified under product code DBL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KALLESTAD FLORESCENT ANA/AMA/ASMA TEST?

KALLESTAD FLORESCENT ANA/AMA/ASMA TEST is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K792610.

When did KALLESTAD FLORESCENT ANA/AMA/ASMA TEST receive FDA 510(k) clearance?

KALLESTAD FLORESCENT ANA/AMA/ASMA TEST received FDA 510(k) clearance on 1980-02-22, under 510(k) number K792610.

Who is the listed applicant for KALLESTAD FLORESCENT ANA/AMA/ASMA TEST?

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

What is the FDA product code for KALLESTAD FLORESCENT ANA/AMA/ASMA TEST?

The FDA product code for KALLESTAD FLORESCENT ANA/AMA/ASMA TEST is DBL.

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Related Devices (Code: DBL)

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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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