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FDA 510(k)

CAPITOL URINE DRUG SCREEN COLLECTION KIT

K-Number: K951122 · 1995-05-05

ApplicantHarry A. Schlakman
Decision Date1995-05-05
Product CodeKDW
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CAPITOL URINE DRUG SCREEN COLLECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Harry A. Schlakman. It received FDA 510(k) clearance on 1995-05-05 under 510(k) number K951122. The device is classified under product code KDW. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPITOL URINE DRUG SCREEN COLLECTION KIT?

CAPITOL URINE DRUG SCREEN COLLECTION KIT is a medical device that received FDA 510(k) clearance on 1995-05-05. The listed applicant is Harry A. Schlakman. The 510(k) number is K951122.

When did CAPITOL URINE DRUG SCREEN COLLECTION KIT receive FDA 510(k) clearance?

CAPITOL URINE DRUG SCREEN COLLECTION KIT received FDA 510(k) clearance on 1995-05-05, under 510(k) number K951122.

Who is the listed applicant for CAPITOL URINE DRUG SCREEN COLLECTION KIT?

The FDA 510(k) record lists Harry A. Schlakman as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPITOL URINE DRUG SCREEN COLLECTION KIT?

The FDA product code for CAPITOL URINE DRUG SCREEN COLLECTION KIT is KDW.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Harry A. Schlakman 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.

K945480MOSS(R) STEEL BREAKAWAY(R) INTRODUCER

Related Devices (Code: KDW)

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.

K970580SASI-DC1TSSubstance Abuse Specialties, Inc.K931474DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITSGbf Medical GroupK913967DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEMDoxtech, 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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