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FDA 510(k)

DIALYSIS DRAINAGE UNIT, PERITONEAL

K-Number: K772150 · 1977-11-28

ApplicantC.R. Bard, Inc.
Decision Date1977-11-28
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYSIS DRAINAGE UNIT, PERITONEAL 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 1977-11-28 under 510(k) number K772150. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYSIS DRAINAGE UNIT, PERITONEAL?

DIALYSIS DRAINAGE UNIT, PERITONEAL is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K772150.

When did DIALYSIS DRAINAGE UNIT, PERITONEAL receive FDA 510(k) clearance?

DIALYSIS DRAINAGE UNIT, PERITONEAL received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772150.

Who is the listed applicant for DIALYSIS DRAINAGE UNIT, PERITONEAL?

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 DIALYSIS DRAINAGE UNIT, PERITONEAL?

The FDA product code for DIALYSIS DRAINAGE UNIT, PERITONEAL is FKX.

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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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