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FDA 510(k)

AUTOMATIC FILM PROCESSORIO M. R80

K-Number: K781068 · 1978-07-17

ApplicantTecnomed, Inc.
Decision Date1978-07-17
Product CodeIWX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC FILM PROCESSORIO M. R80 is the device name listed in this FDA 510(k) record. The listed applicant is Tecnomed, Inc.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K781068. The device is classified under product code IWX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC FILM PROCESSORIO M. R80?

AUTOMATIC FILM PROCESSORIO M. R80 is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Tecnomed, Inc.. The 510(k) number is K781068.

When did AUTOMATIC FILM PROCESSORIO M. R80 receive FDA 510(k) clearance?

AUTOMATIC FILM PROCESSORIO M. R80 received FDA 510(k) clearance on 1978-07-17, under 510(k) number K781068.

Who is the listed applicant for AUTOMATIC FILM PROCESSORIO M. R80?

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

What is the FDA product code for AUTOMATIC FILM PROCESSORIO M. R80?

The FDA product code for AUTOMATIC FILM PROCESSORIO M. R80 is IWX.

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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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