BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES— 510(k) K020538
Substantially EquivalentBoehringer Laboratories
FDA 510(k) clearance K020538 for BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES, Substantially Equivalent on 2002-05-15. Applicant: Boehringer Laboratories.
Clearance details
- Applicant
- Boehringer Laboratories
- Product code
- Code DWL
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norristown, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.