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FDA 510(k)

CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T

K-Number: K072453 · 2007-12-03

ApplicantBrymill Corp.
Decision Date2007-12-03
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T is the device name listed in this FDA 510(k) record. The listed applicant is Brymill Corp.. It received FDA 510(k) clearance on 2007-12-03 under 510(k) number K072453. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T?

CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T is a medical device that received FDA 510(k) clearance on 2007-12-03. The listed applicant is Brymill Corp.. The 510(k) number is K072453.

When did CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T receive FDA 510(k) clearance?

CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T received FDA 510(k) clearance on 2007-12-03, under 510(k) number K072453.

Who is the listed applicant for CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T?

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

What is the FDA product code for CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T?

The FDA product code for CRY-AC TRACKER, MODEL(S) B-700T, AND B-800T is GEH.

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Other records listing Brymill Corp. as applicant

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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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