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FDA 510(k)

MTI PHOTOSCREENER

K-Number: K934880 · 1994-04-06

ApplicantMedical Technology and Innovations, Inc.
Decision Date1994-04-06
Product CodeMMF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MTI PHOTOSCREENER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technology and Innovations, Inc.. It received FDA 510(k) clearance on 1994-04-06 under 510(k) number K934880. The device is classified under product code MMF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTI PHOTOSCREENER?

MTI PHOTOSCREENER is a medical device that received FDA 510(k) clearance on 1994-04-06. The listed applicant is Medical Technology and Innovations, Inc.. The 510(k) number is K934880.

When did MTI PHOTOSCREENER receive FDA 510(k) clearance?

MTI PHOTOSCREENER received FDA 510(k) clearance on 1994-04-06, under 510(k) number K934880.

Who is the listed applicant for MTI PHOTOSCREENER?

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

What is the FDA product code for MTI PHOTOSCREENER?

The FDA product code for MTI PHOTOSCREENER is MMF.

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Other records listing Medical Technology and Innovations, 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.

K020512MTI ST#1 SILICONE PESSARYK854354THE BLEDSOE PASSIVE MOTION EXERCISER

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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