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FDA 510(k)

CHOY COMPRESSION FRAME

K-Number: K070968 · 2007-11-15

ApplicantChoy Medical Technologies, Inc.
Decision Date2007-11-15
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHOY COMPRESSION FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Choy Medical Technologies, Inc.. It received FDA 510(k) clearance on 2007-11-15 under 510(k) number K070968. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOY COMPRESSION FRAME?

CHOY COMPRESSION FRAME is a medical device that received FDA 510(k) clearance on 2007-11-15. The listed applicant is Choy Medical Technologies, Inc.. The 510(k) number is K070968.

When did CHOY COMPRESSION FRAME receive FDA 510(k) clearance?

CHOY COMPRESSION FRAME received FDA 510(k) clearance on 2007-11-15, under 510(k) number K070968.

Who is the listed applicant for CHOY COMPRESSION FRAME?

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

What is the FDA product code for CHOY COMPRESSION FRAME?

The FDA product code for CHOY COMPRESSION FRAME is LNH.

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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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