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FDA 510(k)

QUANTIMETRIX URINE DIPSTICK CONTROL

K-Number: K874890 · 1988-01-21

ApplicantQuantimetrix Medical Industries
Decision Date1988-01-21
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTIMETRIX URINE DIPSTICK CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Quantimetrix Medical Industries. It received FDA 510(k) clearance on 1988-01-21 under 510(k) number K874890. The device is classified under product code JJW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTIMETRIX URINE DIPSTICK CONTROL?

QUANTIMETRIX URINE DIPSTICK CONTROL is a medical device that received FDA 510(k) clearance on 1988-01-21. The listed applicant is Quantimetrix Medical Industries. The 510(k) number is K874890.

When did QUANTIMETRIX URINE DIPSTICK CONTROL receive FDA 510(k) clearance?

QUANTIMETRIX URINE DIPSTICK CONTROL received FDA 510(k) clearance on 1988-01-21, under 510(k) number K874890.

Who is the listed applicant for QUANTIMETRIX URINE DIPSTICK CONTROL?

The FDA 510(k) record lists Quantimetrix Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTIMETRIX URINE DIPSTICK CONTROL?

The FDA product code for QUANTIMETRIX URINE DIPSTICK CONTROL is JJW.

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Other records listing Quantimetrix Medical Industries 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.

K895778QUANTIMETRIX BILIRUBIN CALIBRATORSK883395ALKPHOR(TM) SYSTEM, HUMAN SERUM ALKA PHOS ISOENZYK883247LIPOPHOR(TM) SYST, HUMAN SERUM LIPOPROTEIN CONTROLK874302QUANTIMETRIX TOTAL CREATINE KINASE CONTROLK873011QUANTIMETRIX SERUM ALCOHOL CONTROL LEVEL 1 AND 2K873467QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL

View all 8 devices →

Related Devices (Code: JJW)

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.

K170091UA-Cellular CompleteStreckK110846RANDOX URINALYSIS CONTROLS, LEVELS 1 AND 2Randox Laboratories LimitedK103387MISSION LIQUID URINE CONTROL, MISSION LIQUID DIPTUBE URINE CONTROL, MISSION DRY STRIP URINE CONTROLACON Laboratories, Inc.K081908CLINIQA LIQUID QC URINALYSIS CONTROLS, LEVELS 1 AND 2Cliniqa CorporationK072640IRISPEC,CA/CB/CCIris DiagnosticsK070848LIQUICHEK URINALYSIS CONTROL (BI-LEVEL), CONTROL LEVEL1, LEVEL 2,MINIPAK, 435,436,437,435XBio-Rad, Diagnostics Grp.

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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