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FDA 510(k)

MEDICAL MULTI-IMAGE CAMERA-676

K-Number: K850184 · 1985-02-21

ApplicantDunn Instruments, Inc.
Decision Date1985-02-21
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDICAL MULTI-IMAGE CAMERA-676 is the device name listed in this FDA 510(k) record. The listed applicant is Dunn Instruments, Inc.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850184. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL MULTI-IMAGE CAMERA-676?

MEDICAL MULTI-IMAGE CAMERA-676 is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Dunn Instruments, Inc.. The 510(k) number is K850184.

When did MEDICAL MULTI-IMAGE CAMERA-676 receive FDA 510(k) clearance?

MEDICAL MULTI-IMAGE CAMERA-676 received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850184.

Who is the listed applicant for MEDICAL MULTI-IMAGE CAMERA-676?

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

What is the FDA product code for MEDICAL MULTI-IMAGE CAMERA-676?

The FDA product code for MEDICAL MULTI-IMAGE CAMERA-676 is LMC.

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Other records listing Dunn Instruments, 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.

K781214CAMERAS, MULTI-IMAGEK771924HEARTBEATER

Related Devices (Code: LMC)

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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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