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FDA 510(k)

BLOOD MONITOR BMM 10-4

K-Number: K831404 · 1984-04-25

ApplicantGambro, Inc.
Decision Date1984-04-25
Product CodeLLB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLOOD MONITOR BMM 10-4 is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K831404. The device is classified under product code LLB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD MONITOR BMM 10-4?

BLOOD MONITOR BMM 10-4 is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Gambro, Inc.. The 510(k) number is K831404.

When did BLOOD MONITOR BMM 10-4 receive FDA 510(k) clearance?

BLOOD MONITOR BMM 10-4 received FDA 510(k) clearance on 1984-04-25, under 510(k) number K831404.

Who is the listed applicant for BLOOD MONITOR BMM 10-4?

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

What is the FDA product code for BLOOD MONITOR BMM 10-4?

The FDA product code for BLOOD MONITOR BMM 10-4 is LLB.

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Other records listing Gambro, Inc. as applicant

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.

K083158EXALIS, SOFTWARE VERSION 1.15K070643PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35K032431PRISMA M60/M100 SETSK896758GAMBRO BICARBONATE MONITOR BCM 10-3K896757GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWSK902481GAMBRO ALWALL GFS PLUS 11, 16 & 20 HOLLOW FIBER

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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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