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FDA 510(k)

FOLEY CATHETER TUBE HOLDER NO. 101

K-Number: K924567 · 1992-11-23

ApplicantAnsley Medical Products, Inc.
Decision Date1992-11-23
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FOLEY CATHETER TUBE HOLDER NO. 101 is the device name listed in this FDA 510(k) record. The listed applicant is Ansley Medical Products, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K924567. 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 FOLEY CATHETER TUBE HOLDER NO. 101?

FOLEY CATHETER TUBE HOLDER NO. 101 is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Ansley Medical Products, Inc.. The 510(k) number is K924567.

When did FOLEY CATHETER TUBE HOLDER NO. 101 receive FDA 510(k) clearance?

FOLEY CATHETER TUBE HOLDER NO. 101 received FDA 510(k) clearance on 1992-11-23, under 510(k) number K924567.

Who is the listed applicant for FOLEY CATHETER TUBE HOLDER NO. 101?

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

What is the FDA product code for FOLEY CATHETER TUBE HOLDER NO. 101?

The FDA product code for FOLEY CATHETER TUBE HOLDER NO. 101 is KMK.

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Other records listing Ansley Medical Products, 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.

K932857ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.K925290CATALOG NUMBER 111 (FACESHIELD)K924566RESTRAINT, PROTECTIVE N0. 103K924568TUBE, LEAD, AND CORD HOLDER NO. 102

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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