STERILE URETHRAL CATHETER PROCEDURE KITS— 510(k) K903340

Unknown

Superior Healthcare Group, Inc.

FDA 510(k) clearance K903340 for STERILE URETHRAL CATHETER PROCEDURE KITS, Unknown on 1990-10-04. Applicant: Superior Healthcare Group, Inc.. Device class: 2.

Clearance details

Applicant
Superior Healthcare Group, Inc.
Product code
Code FCM
Device class
Class 2
Regulation
21 CFR 876.5130
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Cumberland, RI, US
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Recalls naming K903340

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K903340.

Data sourced from openFDA. This site is unofficial and independent of the FDA.