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FDA 510(k)

BENTLEY-TRANTEC DISPOS. DOMES D-260-

K-Number: K841811 · 1985-09-09

ApplicantAmerican Bentley
Decision Date1985-09-09
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BENTLEY-TRANTEC DISPOS. DOMES D-260- is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1985-09-09 under 510(k) number K841811. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENTLEY-TRANTEC DISPOS. DOMES D-260-?

BENTLEY-TRANTEC DISPOS. DOMES D-260- is a medical device that received FDA 510(k) clearance on 1985-09-09. The listed applicant is American Bentley. The 510(k) number is K841811.

When did BENTLEY-TRANTEC DISPOS. DOMES D-260- receive FDA 510(k) clearance?

BENTLEY-TRANTEC DISPOS. DOMES D-260- received FDA 510(k) clearance on 1985-09-09, under 510(k) number K841811.

Who is the listed applicant for BENTLEY-TRANTEC DISPOS. DOMES D-260-?

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

What is the FDA product code for BENTLEY-TRANTEC DISPOS. DOMES D-260-?

The FDA product code for BENTLEY-TRANTEC DISPOS. DOMES D-260- is DRS.

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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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