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FDA 510(k)

ALARM

K-Number: K790559 · 1979-06-01

ApplicantMaddak, Inc.
Decision Date1979-06-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1979-06-01 under 510(k) number K790559. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALARM?

ALARM is a medical device that received FDA 510(k) clearance on 1979-06-01. The listed applicant is Maddak, Inc.. The 510(k) number is K790559.

When did ALARM receive FDA 510(k) clearance?

ALARM received FDA 510(k) clearance on 1979-06-01, under 510(k) number K790559.

Who is the listed applicant for ALARM?

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

What is the FDA product code for ALARM?

The FDA product code for ALARM is FRN.

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Other records listing Maddak, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FRN)

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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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