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FDA 510(k)

FOLEY CATHETERIZATION TRAY

K-Number: K790254 · 1979-04-10

ApplicantSnyder Laboratories, Inc.
Decision Date1979-04-10
Product CodeFCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FOLEY CATHETERIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Laboratories, Inc.. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790254. 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 FOLEY CATHETERIZATION TRAY?

FOLEY CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K790254.

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

FOLEY CATHETERIZATION TRAY received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790254.

Who is the listed applicant for FOLEY CATHETERIZATION TRAY?

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

What is the FDA product code for FOLEY CATHETERIZATION TRAY?

The FDA product code for FOLEY CATHETERIZATION TRAY is FCM.

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Related Devices (Code: FCM)

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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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