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FDA 510(k)

LOG-A-RYTHM MODEL 100 AND MODEL 1001

K-Number: K952790 · 1996-10-17

ApplicantNian-Crae, Inc.
Decision Date1996-10-17
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LOG-A-RYTHM MODEL 100 AND MODEL 1001 is the device name listed in this FDA 510(k) record. The listed applicant is Nian-Crae, Inc.. It received FDA 510(k) clearance on 1996-10-17 under 510(k) number K952790. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOG-A-RYTHM MODEL 100 AND MODEL 1001?

LOG-A-RYTHM MODEL 100 AND MODEL 1001 is a medical device that received FDA 510(k) clearance on 1996-10-17. The listed applicant is Nian-Crae, Inc.. The 510(k) number is K952790.

When did LOG-A-RYTHM MODEL 100 AND MODEL 1001 receive FDA 510(k) clearance?

LOG-A-RYTHM MODEL 100 AND MODEL 1001 received FDA 510(k) clearance on 1996-10-17, under 510(k) number K952790.

Who is the listed applicant for LOG-A-RYTHM MODEL 100 AND MODEL 1001?

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

What is the FDA product code for LOG-A-RYTHM MODEL 100 AND MODEL 1001?

The FDA product code for LOG-A-RYTHM MODEL 100 AND MODEL 1001 is DRT.

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Related Devices (Code: DRT)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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