FDA 510(k)

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE

K-Number: K990761 · 1999-07-09

Decision Date1999-07-09

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Tuttnauer U.S.A Co, Ltd.. It received FDA 510(k) clearance on 1999-07-09 under 510(k) number K990761. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE?

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE is a medical device that received FDA 510(k) clearance on 1999-07-09. The listed applicant is Tuttnauer U.S.A Co, Ltd.. The 510(k) number is K990761.

When did TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE receive FDA 510(k) clearance?

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE received FDA 510(k) clearance on 1999-07-09, under 510(k) number K990761.

Who is the listed applicant for TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE?

The FDA 510(k) record lists Tuttnauer U.S.A Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE?

The FDA product code for TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE is FRG.

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Other records listing Tuttnauer U.S.A Co, Ltd. as applicant

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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.