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FDA 510(k)

URINARY VMA - SCREEN TEST KIT

K-Number: K772151 · 1977-11-30

ApplicantEppendorf-Brinkmann, Inc.
Decision Date1977-11-30
Product CodeCDF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URINARY VMA - SCREEN TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Eppendorf-Brinkmann, Inc.. It received FDA 510(k) clearance on 1977-11-30 under 510(k) number K772151. The device is classified under product code CDF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY VMA - SCREEN TEST KIT?

URINARY VMA - SCREEN TEST KIT is a medical device that received FDA 510(k) clearance on 1977-11-30. The listed applicant is Eppendorf-Brinkmann, Inc.. The 510(k) number is K772151.

When did URINARY VMA - SCREEN TEST KIT receive FDA 510(k) clearance?

URINARY VMA - SCREEN TEST KIT received FDA 510(k) clearance on 1977-11-30, under 510(k) number K772151.

Who is the listed applicant for URINARY VMA - SCREEN TEST KIT?

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

What is the FDA product code for URINARY VMA - SCREEN TEST KIT?

The FDA product code for URINARY VMA - SCREEN TEST KIT is CDF.

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Other records listing Eppendorf-Brinkmann, 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.

K780819GLYCOHEMOGLOBIN-SKREEN TEST KITK772337URINARY 17-KETOSTERIOD/17K761271URIN. L7-OH CORTICOSTEROID T(NON HYDRO)

Related Devices (Code: CDF)

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.

K953077PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEMBeckman Instruments, Inc.K934977MODEL 5500 CEASEsa, Inc.K895288HVA EIA KIT YAMASAYamasa Shoy Co., Ltd.K895287VMA EIA KIT YAMASAYamasa Shoy Co., Ltd.K873372HVA & HOMOVANILLIC ACID BY HPLC METHODBio-RadK861962VANILMANDELIC ACID (VMA) REAGENT SETSterling 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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