VERSA-VIAL— 510(k) K920177
Substantially EquivalentBioteque America, Inc.
FDA 510(k) clearance K920177 for VERSA-VIAL, Substantially Equivalent on 1992-07-13. Applicant: Bioteque America, Inc..
Clearance details
- Applicant
- Bioteque America, Inc.
- Product code
- Code DQF
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Levittown, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.