VESSEL DILATORS— 510(k) K910502
Substantially EquivalentAkcess Medical Products, Inc.
FDA 510(k) clearance K910502 for VESSEL DILATORS, Substantially Equivalent on 1991-04-29. Applicant: Akcess Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Akcess Medical Products, Inc.
- Product code
- Code FKA
- Device class
- Class 2
- Regulation
- 21 CFR 876.5540
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Brunswick, NJ, US
Recent devices under product code FKA
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