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FDA 510(k)

BECKMAN MA MICROALBUMIN REAGENT KIT

K-Number: K895883 · 1989-12-27

ApplicantBeckman Instruments, Inc.
Decision Date1989-12-27
Product CodeJIQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN MA MICROALBUMIN REAGENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K895883. The device is classified under product code JIQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN MA MICROALBUMIN REAGENT KIT?

BECKMAN MA MICROALBUMIN REAGENT KIT is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K895883.

When did BECKMAN MA MICROALBUMIN REAGENT KIT receive FDA 510(k) clearance?

BECKMAN MA MICROALBUMIN REAGENT KIT received FDA 510(k) clearance on 1989-12-27, under 510(k) number K895883.

Who is the listed applicant for BECKMAN MA MICROALBUMIN REAGENT KIT?

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

What is the FDA product code for BECKMAN MA MICROALBUMIN REAGENT KIT?

The FDA product code for BECKMAN MA MICROALBUMIN REAGENT KIT is JIQ.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JIQ)

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.

K013643AUSAM TOTAL ALBUMIN ASSAYAusam Biotecthnologies, Inc.K991800HEMOCHEK URINE COLLECTION KITOsborn Group, Inc.K971458ENZIP IMMUNOTURBIDIMETRIC MICROALBUMIN ASSAY KITDiagnostic SpecialtiesK965035IMMAGE IMMUNOCHEMISTRY SYSTEM MICROALBUMIN (MA) REAGENTBeckman Instruments, Inc.K944664WAKO MICRO-ALBUMIN B/WAKO MICRO ALBUMIN CALIBRATORWako Chemicals USA, Inc.K936202URINARY ALBUMIN TEST PACKDupont Medical Products

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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