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FDA 510(k)

MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F

K-Number: K050558 · 2005-08-29

ApplicantC.R. Bard, Inc.
Decision Date2005-08-29
Product CodeDTK
Advisory CommitteeCV
DecisionUnknown

Device Summary

MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F 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 2005-08-29 under 510(k) number K050558. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F?

MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F is a medical device that received FDA 510(k) clearance on 2005-08-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K050558.

When did MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F receive FDA 510(k) clearance?

MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F received FDA 510(k) clearance on 2005-08-29, under 510(k) number K050558.

Who is the listed applicant for MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F?

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 MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F?

The FDA product code for MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F 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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