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FDA 510(k)

ALLERCOAT ALLERGEN DISCS

K-Number: K842125 · 1984-06-07

ApplicantKallestad Laboratories, Inc.
Decision Date1984-06-07
Product CodeDGC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ALLERCOAT ALLERGEN DISCS 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 1984-06-07 under 510(k) number K842125. The device is classified under product code DGC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLERCOAT ALLERGEN DISCS?

ALLERCOAT ALLERGEN DISCS is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K842125.

When did ALLERCOAT ALLERGEN DISCS receive FDA 510(k) clearance?

ALLERCOAT ALLERGEN DISCS received FDA 510(k) clearance on 1984-06-07, under 510(k) number K842125.

Who is the listed applicant for ALLERCOAT ALLERGEN DISCS?

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 ALLERCOAT ALLERGEN DISCS?

The FDA product code for ALLERCOAT ALLERGEN DISCS is DGC.

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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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