ROBICSEK PROBE/RETRACTOR— 510(k) K910682
Substantially EquivalentBio-Vascular, Inc.
FDA 510(k) clearance K910682 for ROBICSEK PROBE/RETRACTOR, Substantially Equivalent on 1991-05-08. Applicant: Bio-Vascular, Inc.. Device class: 2.
Clearance details
- Applicant
- Bio-Vascular, Inc.
- Product code
- Code DWP
- Device class
- Class 2
- Regulation
- 21 CFR 870.4475
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.