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Boehringer Laboratories Pneumatic Ambulatory Compression System 8200 Series
FDA 510(k)Class II (US FDA 510(k))
510(k) K020538
Identifiers
- 510(k) Number
- K020538 FDA 510(k)
- FDA Product Code
- DWL FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 880.5780 FDA 510(k)
- Regulation Number
- 880.5780 FDA 510(k)
- Advisory Committee
- General Hospital FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Boehringer Laboratories Pneumatic Ambulatory Compression System 8200 Series by Boehringer Laboratories, Llc — Class II — FDA_510K — listed in FDA 510(k)
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K020538 | Class II | Active |
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Manufacturer
- Manufacturer
- Boehringer Laboratories, Llc
- FDA Applicant
- Boehringer Laboratories
Sources (1)
- FDA 510(k) K020538 24 fields · synced Jun 18, 2026