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FDA 510(k)

HEMA(PRO)TEC(TION)

K-Number: K885324 · 1989-02-17

ApplicantMedical Products Search, Inc.
Decision Date1989-02-17
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HEMA(PRO)TEC(TION) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Products Search, Inc.. It received FDA 510(k) clearance on 1989-02-17 under 510(k) number K885324. 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 HEMA(PRO)TEC(TION)?

HEMA(PRO)TEC(TION) is a medical device that received FDA 510(k) clearance on 1989-02-17. The listed applicant is Medical Products Search, Inc.. The 510(k) number is K885324.

When did HEMA(PRO)TEC(TION) receive FDA 510(k) clearance?

HEMA(PRO)TEC(TION) received FDA 510(k) clearance on 1989-02-17, under 510(k) number K885324.

Who is the listed applicant for HEMA(PRO)TEC(TION)?

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

What is the FDA product code for HEMA(PRO)TEC(TION)?

The FDA product code for HEMA(PRO)TEC(TION) is GIO.

Other records listing Medical Products Search, 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.

K905665PATIENT EXAMINATION GLOVESK874454IV-PUSH, CONSTANT INFUSION PUMP

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.

K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMInnovative Medical Technologies, Inc.K941291MONOJECT SAMPLETTE SEPARATOR TUBESherwood Medical Co.K894851TRU-TRAXHumagen, 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

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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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