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FDA 510(k)

DAVOL ARTHRO-FLO 3

K-Number: K951026 · 1995-06-02

ApplicantDavol Inc., Sub. C. R. Bard, Inc.
Decision Date1995-06-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DAVOL ARTHRO-FLO 3 is the device name listed in this FDA 510(k) record. The listed applicant is Davol Inc., Sub. C. R. Bard, Inc.. It received FDA 510(k) clearance on 1995-06-02 under 510(k) number K951026. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL ARTHRO-FLO 3?

DAVOL ARTHRO-FLO 3 is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is Davol Inc., Sub. C. R. Bard, Inc.. The 510(k) number is K951026.

When did DAVOL ARTHRO-FLO 3 receive FDA 510(k) clearance?

DAVOL ARTHRO-FLO 3 received FDA 510(k) clearance on 1995-06-02, under 510(k) number K951026.

Who is the listed applicant for DAVOL ARTHRO-FLO 3?

The FDA 510(k) record lists Davol Inc., Sub. C. R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAVOL ARTHRO-FLO 3?

The FDA product code for DAVOL ARTHRO-FLO 3 is HRX.

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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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