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FDA 510(k)

BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V

K-Number: K090265 · 2009-05-15

ApplicantScican , Ltd.
Decision Date2009-05-15
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V is the device name listed in this FDA 510(k) record. The listed applicant is Scican , Ltd.. It received FDA 510(k) clearance on 2009-05-15 under 510(k) number K090265. 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 BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V?

BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V is a medical device that received FDA 510(k) clearance on 2009-05-15. The listed applicant is Scican , Ltd.. The 510(k) number is K090265.

When did BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V receive FDA 510(k) clearance?

BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V received FDA 510(k) clearance on 2009-05-15, under 510(k) number K090265.

Who is the listed applicant for BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V?

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

What is the FDA product code for BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V?

The FDA product code for BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V is FLE.

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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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