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FDA 510(k)

QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM

K-Number: K972969 · 1997-09-22

ApplicantInnovative Medical Technologies, Inc.
Decision Date1997-09-22
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Technologies, Inc.. It received FDA 510(k) clearance on 1997-09-22 under 510(k) number K972969. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM?

QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1997-09-22. The listed applicant is Innovative Medical Technologies, Inc.. The 510(k) number is K972969.

When did QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM receive FDA 510(k) clearance?

QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM received FDA 510(k) clearance on 1997-09-22, under 510(k) number K972969.

Who is the listed applicant for QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM?

The FDA 510(k) record lists Innovative Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM?

The FDA product code for QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM is GIO.

Related Clinical Trials

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Other records listing Innovative Medical Technologies, 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.

K220458UltraFlo-R Push Button Blood Collection SetK123987IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SETK936087CARPAL BOXK904237RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEMK854194IMT ULTRASONIC STRIDE MONITOR

Related Devices (Code: GIO)

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.

K941291MONOJECT SAMPLETTE SEPARATOR TUBESherwood Medical Co.K894851TRU-TRAXHumagen, Inc.K885324HEMA(PRO)TEC(TION)Medical Products Search, Inc.K885138CAPILLARY TUBE, BLOOD COLLECTIONCoeur Laboratories, Inc.K884623SAFE-TEC CAPILLARY BLOOD COLLECTION TUBESafe-Tec Clinical Products, Inc.K881262CARAWAY TUBES, HEPARIN AND PLAINHelps Products, 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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