LAKE MALE EXTERNAL CATHETERIZATION KIT— 510(k) K902508
UnknownLake Medical Products, Inc.
FDA 510(k) clearance K902508 for LAKE MALE EXTERNAL CATHETERIZATION KIT, Unknown on 1990-08-23. Applicant: Lake Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Lake Medical Products, 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
- St. Louis, MO, US
Recent devices under product code FCM
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