HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM— 510(k) K894892
Substantially EquivalentKoven and Assoc., Inc.
FDA 510(k) clearance K894892 for HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM, Substantially Equivalent on 1989-10-27. Applicant: Koven and Assoc., Inc.. Device class: 2.
Clearance details
- Applicant
- Koven and Assoc., Inc.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
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