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FDA 510(k)

NHMC FOLEY CATHETERIZATION TRAY

K-Number: K960566 · 1996-02-29

ApplicantNational Healthcare Mfg. Corp.
Decision Date1996-02-29
Product CodeFCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NHMC FOLEY CATHETERIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is National Healthcare Mfg. Corp.. It received FDA 510(k) clearance on 1996-02-29 under 510(k) number K960566. The device is classified under product code FCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NHMC FOLEY CATHETERIZATION TRAY?

NHMC FOLEY CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is National Healthcare Mfg. Corp.. The 510(k) number is K960566.

When did NHMC FOLEY CATHETERIZATION TRAY receive FDA 510(k) clearance?

NHMC FOLEY CATHETERIZATION TRAY received FDA 510(k) clearance on 1996-02-29, under 510(k) number K960566.

Who is the listed applicant for NHMC FOLEY CATHETERIZATION TRAY?

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

What is the FDA product code for NHMC FOLEY CATHETERIZATION TRAY?

The FDA product code for NHMC FOLEY CATHETERIZATION TRAY is FCM.

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Other records listing National Healthcare Mfg. 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.

K972013NATIONAL MEDICAL HEALTHCARE CUSTOM OB/GYN KITS, TRAYS, OR PACKSK971465NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYSK971317NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYSK962670NHMC IRRIGATION TRAYK962254NHMC URETHRAL CATHETERIZATION TRAYK960523NHMC DRESSING TRAY

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Related Devices (Code: FCM)

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.

K254076BD Touchless™ Plus Unisex Pre-Lubricated Urethral Catheter KitC.R. Bard, Inc.K250891Cure Catheter Insertion Kit (K1); Cure Catheter Insertion Kit (K2); Cure Catheter Insertion Kit (K2-90); Cure Catheter Insertion Kit (K3); Cure Hydrophilic Catheter Kit (HM12UK); Cure Hydrophilic Catheter Kit (HM14UK); Cure Hydrophilic Catheter Kit (HM16UK); Cure Pocket Catheter Kit (M14UK); Cure Catheter Closed System Kit (CS8); Cure Catheter Closed System Kit (CS10); Cure Catheter Closed System Kit (CS12); Cure Catheter Closed System Kit (CS14); Cure Catheter Closed System Kit (CS14CConvatec LimitedK223821Self-Cath Closed SystemColoplastK082831AMSELF CLOSED CATHETERIZATION SYSTEMAmsino International, Inc.K070939SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEMColoplast Manufacturing Us, LLCK070048GUARDIAN CATHETER-INFANT URINARY COLLECTION KITMarian Medical, 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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