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FDA 510(k)

RECOVERY FILTER SYSTEM, MODEL RF-048F

K-Number: K022236 · 2002-11-27

ApplicantC.R. Bard, Inc.
Decision Date2002-11-27
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECOVERY FILTER SYSTEM, MODEL RF-048F is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2002-11-27 under 510(k) number K022236. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECOVERY FILTER SYSTEM, MODEL RF-048F?

RECOVERY FILTER SYSTEM, MODEL RF-048F is a medical device that received FDA 510(k) clearance on 2002-11-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K022236.

When did RECOVERY FILTER SYSTEM, MODEL RF-048F receive FDA 510(k) clearance?

RECOVERY FILTER SYSTEM, MODEL RF-048F received FDA 510(k) clearance on 2002-11-27, under 510(k) number K022236.

Who is the listed applicant for RECOVERY FILTER SYSTEM, MODEL RF-048F?

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

What is the FDA product code for RECOVERY FILTER SYSTEM, MODEL RF-048F?

The FDA product code for RECOVERY FILTER SYSTEM, MODEL RF-048F is DTK.

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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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