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FDA 510(k)

TIMLEINE(TM) VENIPUNCTURE SYSTEM

K-Number: K870770 · 1987-04-23

ApplicantIpax, Inc.
Decision Date1987-04-23
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TIMLEINE(TM) VENIPUNCTURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ipax, Inc.. It received FDA 510(k) clearance on 1987-04-23 under 510(k) number K870770. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIMLEINE(TM) VENIPUNCTURE SYSTEM?

TIMLEINE(TM) VENIPUNCTURE SYSTEM is a medical device that received FDA 510(k) clearance on 1987-04-23. The listed applicant is Ipax, Inc.. The 510(k) number is K870770.

When did TIMLEINE(TM) VENIPUNCTURE SYSTEM receive FDA 510(k) clearance?

TIMLEINE(TM) VENIPUNCTURE SYSTEM received FDA 510(k) clearance on 1987-04-23, under 510(k) number K870770.

Who is the listed applicant for TIMLEINE(TM) VENIPUNCTURE SYSTEM?

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

What is the FDA product code for TIMLEINE(TM) VENIPUNCTURE SYSTEM?

The FDA product code for TIMLEINE(TM) VENIPUNCTURE SYSTEM is KMK.

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Other records listing Ipax, Inc. as applicant

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K200893ProntoPump Sterile Tube SetK971242BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28)K971245BLINK EXTERNAL EYELID WEIGHTK915158SUREBREATH DOME, E-Z BREATHERK915118PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBEK914221KPE 220 TS, NONSTERILE

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Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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