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FDA 510(k)

DIAPACT CRRT

K-Number: K973322 · 1998-11-10

ApplicantB.Braun Medical, Inc.
Decision Date1998-11-10
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIAPACT CRRT is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1998-11-10 under 510(k) number K973322. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAPACT CRRT?

DIAPACT CRRT is a medical device that received FDA 510(k) clearance on 1998-11-10. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K973322.

When did DIAPACT CRRT receive FDA 510(k) clearance?

DIAPACT CRRT received FDA 510(k) clearance on 1998-11-10, under 510(k) number K973322.

Who is the listed applicant for DIAPACT CRRT?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAPACT CRRT?

The FDA product code for DIAPACT CRRT is KDI.

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Related Devices (Code: KDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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