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FDA 510(k)

IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS

K-Number: K912531 · 1991-09-04

ApplicantInnovative Medical Devices, Inc.
Decision Date1991-09-04
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Devices, Inc.. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K912531. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS?

IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Innovative Medical Devices, Inc.. The 510(k) number is K912531.

When did IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS receive FDA 510(k) clearance?

IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS received FDA 510(k) clearance on 1991-09-04, under 510(k) number K912531.

Who is the listed applicant for IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS?

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

What is the FDA product code for IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS?

The FDA product code for IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS is FET.

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Related Devices (Code: FET)

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

View on FDA Database →

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

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