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FDA 510(k)

TUTTNAUER TABLE-TOP AUTOCLAVE

K-Number: K973550 · 1997-10-29

ApplicantTuttnauer U.S.A Co, Ltd.
Decision Date1997-10-29
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUTTNAUER TABLE-TOP AUTOCLAVE 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 1997-10-29 under 510(k) number K973550. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUTTNAUER TABLE-TOP AUTOCLAVE?

TUTTNAUER TABLE-TOP AUTOCLAVE is a medical device that received FDA 510(k) clearance on 1997-10-29. The listed applicant is Tuttnauer U.S.A Co, Ltd.. The 510(k) number is K973550.

When did TUTTNAUER TABLE-TOP AUTOCLAVE receive FDA 510(k) clearance?

TUTTNAUER TABLE-TOP AUTOCLAVE received FDA 510(k) clearance on 1997-10-29, under 510(k) number K973550.

Who is the listed applicant for TUTTNAUER TABLE-TOP AUTOCLAVE?

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 TABLE-TOP AUTOCLAVE?

The FDA product code for TUTTNAUER TABLE-TOP AUTOCLAVE is FLE.

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

K232658T-Top 10 & T-Top T-Top 11K090783TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVEK032192PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS 4472 EP-1V AND 5596 EP-1VK021504TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540K993856TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EPK990761TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE

View all 8 devices →

Related Devices (Code: FLE)

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.

K261055AMSCO 700 Steam SterilizerSTERIS CorporationK260254Enbio PROEnbio Group AGK252307Getinge GSS67N Series Steam SterilizerMaquet GmbH (A Getinge Group Company)K250168Life Ultra 25L Tabletop Mono Chamber Steam SterilizerLucas LifecareK250164Cassette Autoclave (ACA5)Guangzhou Ajax Medical Equipment Co., Ltd.K243994Steam Sterilizer (2545D)Ningbo Ican Machines Co., Ltd.

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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