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FDA 510(k)

WAKO AUTOKIT APO A1

K-Number: K952615 · 1995-09-08

ApplicantWako Chemicals USA, Inc.
Decision Date1995-09-08
Product CodeJHN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WAKO AUTOKIT APO A1 is the device name listed in this FDA 510(k) record. The listed applicant is Wako Chemicals USA, Inc.. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K952615. The device is classified under product code JHN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WAKO AUTOKIT APO A1?

WAKO AUTOKIT APO A1 is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Wako Chemicals USA, Inc.. The 510(k) number is K952615.

When did WAKO AUTOKIT APO A1 receive FDA 510(k) clearance?

WAKO AUTOKIT APO A1 received FDA 510(k) clearance on 1995-09-08, under 510(k) number K952615.

Who is the listed applicant for WAKO AUTOKIT APO A1?

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

What is the FDA product code for WAKO AUTOKIT APO A1?

The FDA product code for WAKO AUTOKIT APO A1 is JHN.

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Other records listing Wako Chemicals USA, 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.

K100464UTASWAKO I30 (INCLUDES ACCESSORIES), UTASWAKO AFP-L3, CALIBRATOR SET, CONTROL L, CONTROL H, SAMPLE DILUTIONK080125APOLOWAKO T-CHO, HDL-C, TG AND ANALYZER, MODELS 993-23501, 999-23601, 995-23701 AND 993-25201K080123APOLOWAKO HBA1C, GLUCOSE AND ANALYZER, MODELS 993-24601, 991-24401 AND 993-25201K061775WAKO L-TYPE CREATININE-M TEST, AND WAKO CREATININE CALIBRATORK062368WAKO LBA DCP TEST SYSTEM, MODEL 993-05301; DCP CONTROL SET, MODEL 995-0551; DCP CALIBRATOR SET, LIBASYS, MODEL 999-05401K053131WAKO TOTAL BILIRUBIN V, MODELS 410-22701, 998-23291, 416-22801, 990-23191

View all 123 devices →

Related Devices (Code: JHN)

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.

K950383APOLIPOPROTEIN A-I IMMUNOTURBIDIMETRIC KITRandox Laboratories, Ltd.K950382APOLIPOPROTEIN B IMMUNOTURBIDIEMETRIC KITRandox Laboratories, Ltd.K952425OLYMPUS APOLIPOPROTEIN A1 IMMUNOTURBIDIMETRIC REAGENTOlympus America, Inc.K952466OLYMPUS APOLIPOPROTEIN B IMMUNOTURBIDIMETRIC REAGENTOlympus America, Inc.K932603APOLIPOPROTIEN B (APO B)Sigma Diagnostics, Inc.K932606APOLIPOPROTIEN A-1 (APO A-1)Sigma Diagnostics, Inc.

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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