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FDA 510(k)

INTRAVASCULAR CATHETER SECURMENT DEVICE

K-Number: K912211 · 1991-08-09

ApplicantInman Liebelt Corp.
Decision Date1991-08-09
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVASCULAR CATHETER SECURMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Inman Liebelt Corp.. It received FDA 510(k) clearance on 1991-08-09 under 510(k) number K912211. 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 INTRAVASCULAR CATHETER SECURMENT DEVICE?

INTRAVASCULAR CATHETER SECURMENT DEVICE is a medical device that received FDA 510(k) clearance on 1991-08-09. The listed applicant is Inman Liebelt Corp.. The 510(k) number is K912211.

When did INTRAVASCULAR CATHETER SECURMENT DEVICE receive FDA 510(k) clearance?

INTRAVASCULAR CATHETER SECURMENT DEVICE received FDA 510(k) clearance on 1991-08-09, under 510(k) number K912211.

Who is the listed applicant for INTRAVASCULAR CATHETER SECURMENT DEVICE?

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

What is the FDA product code for INTRAVASCULAR CATHETER SECURMENT DEVICE?

The FDA product code for INTRAVASCULAR CATHETER SECURMENT DEVICE is KMK.

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Other records listing Inman Liebelt Corp. 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.

K912146URETERAL CATHETER HOLDERK905590UCEZ - STERILE LENS FOG REDUCTION DEVICEK905583ILC FORCEPS PADSK903611ILC LEG BAG HOLDERK903610O.R. TIP CLEANER

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

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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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