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FDA 510(k)

I.V. LOK TM

K-Number: K770119 · 1977-03-14

ApplicantJelco Laboratories
Decision Date1977-03-14
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. LOK TM is the device name listed in this FDA 510(k) record. The listed applicant is Jelco Laboratories. It received FDA 510(k) clearance on 1977-03-14 under 510(k) number K770119. 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 I.V. LOK TM?

I.V. LOK TM is a medical device that received FDA 510(k) clearance on 1977-03-14. The listed applicant is Jelco Laboratories. The 510(k) number is K770119.

When did I.V. LOK TM receive FDA 510(k) clearance?

I.V. LOK TM received FDA 510(k) clearance on 1977-03-14, under 510(k) number K770119.

Who is the listed applicant for I.V. LOK TM?

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

What is the FDA product code for I.V. LOK TM?

The FDA product code for I.V. LOK TM is KMK.

Other records listing Jelco Laboratories 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.

K791918JELCO WINGED INTRAVASCULAR CATHETERK791372JELCO & KVO CATHETER PLACEMENT UNITK790967CATHETER METAL HUB/RADIOPAQUEK790968CATHETER METAL HUB/NONRADIOPAQUEK790471JELCO* DISC FILTER-0.2 MICRONK790186PROTECTIVSTABILIZER

View all 26 devices →

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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