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FDA 510(k)

DIATHERMY DEVICE-MICROFOCUS

K-Number: K941567 · 1996-04-22

ApplicantCheung Laboratories, Inc.
Decision Date1996-04-22
Product CodeIOA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DIATHERMY DEVICE-MICROFOCUS is the device name listed in this FDA 510(k) record. The listed applicant is Cheung Laboratories, Inc.. It received FDA 510(k) clearance on 1996-04-22 under 510(k) number K941567. The device is classified under product code IOA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIATHERMY DEVICE-MICROFOCUS?

DIATHERMY DEVICE-MICROFOCUS is a medical device that received FDA 510(k) clearance on 1996-04-22. The listed applicant is Cheung Laboratories, Inc.. The 510(k) number is K941567.

When did DIATHERMY DEVICE-MICROFOCUS receive FDA 510(k) clearance?

DIATHERMY DEVICE-MICROFOCUS received FDA 510(k) clearance on 1996-04-22, under 510(k) number K941567.

Who is the listed applicant for DIATHERMY DEVICE-MICROFOCUS?

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

What is the FDA product code for DIATHERMY DEVICE-MICROFOCUS?

The FDA product code for DIATHERMY DEVICE-MICROFOCUS is IOA.

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Related Devices (Code: IOA)

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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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