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FDA 510(k)

CATH-LOK

K-Number: K821957 · 1982-07-28

ApplicantHpd Medical, Inc.
Decision Date1982-07-28
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATH-LOK is the device name listed in this FDA 510(k) record. The listed applicant is Hpd Medical, Inc.. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K821957. 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 CATH-LOK?

CATH-LOK is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Hpd Medical, Inc.. The 510(k) number is K821957.

When did CATH-LOK receive FDA 510(k) clearance?

CATH-LOK received FDA 510(k) clearance on 1982-07-28, under 510(k) number K821957.

Who is the listed applicant for CATH-LOK?

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

What is the FDA product code for CATH-LOK?

The FDA product code for CATH-LOK is KMK.

Other records listing Hpd Medical, 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.

K914994HPD HEATER BASESK895795HPD TUBING CONNECTORSK885314HPD STERILE HUMIDIFYING CHAMBERK864173HPD HUMIDIFYING CHAMBERK841851HPD HUMIDIFIER WICK

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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