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FDA 510(k)

J&S MEDICAL SENTRY URINE DIPSTICK CONTROL

K-Number: K022085 · 2002-07-25

ApplicantJ & S Medical Assoc., Inc.
Decision Date2002-07-25
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

J&S MEDICAL SENTRY URINE DIPSTICK CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is J & S Medical Assoc., Inc.. It received FDA 510(k) clearance on 2002-07-25 under 510(k) number K022085. 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 J&S MEDICAL SENTRY URINE DIPSTICK CONTROL?

J&S MEDICAL SENTRY URINE DIPSTICK CONTROL is a medical device that received FDA 510(k) clearance on 2002-07-25. The listed applicant is J & S Medical Assoc., Inc.. The 510(k) number is K022085.

When did J&S MEDICAL SENTRY URINE DIPSTICK CONTROL receive FDA 510(k) clearance?

J&S MEDICAL SENTRY URINE DIPSTICK CONTROL received FDA 510(k) clearance on 2002-07-25, under 510(k) number K022085.

Who is the listed applicant for J&S MEDICAL SENTRY URINE DIPSTICK CONTROL?

The FDA 510(k) record lists J & S Medical Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for J&S MEDICAL SENTRY URINE DIPSTICK CONTROL?

The FDA product code for J&S MEDICAL SENTRY URINE DIPSTICK CONTROL is JJW.

Related Clinical Trials

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.

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Other records listing J & S Medical Assoc., 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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