FDA 510(k) Premarket Notification K873288: CLOSED FOLEY CATHETER SYSTEM

Submission Details & Decision

Normalized public record details for 510(k) notification K873288.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K873288

Applicant / Sponsor

Todd Medical, Inc.

Device Name

CLOSED FOLEY CATHETER SYSTEM

Product Code

KNY

Decision Date

1987-11-27

Decision / Status

Unknown (SESD)

Advisory Committee

Gastroenterology, Urology (GU)

Clearance Type

Traditional

Third Party Flag

Date Received

1987-08-17

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This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.