RUSCH ENDOTEST CUFF PRESSURE MONITOR— 510(k) K951046
Substantially EquivalentRusch Intl.
FDA 510(k) clearance K951046 for RUSCH ENDOTEST CUFF PRESSURE MONITOR, Substantially Equivalent on 1995-04-06. Applicant: Rusch Intl.. Device class: 2.
Clearance details
- Applicant
- Rusch Intl.
- Product code
- Code BSK
- Device class
- Class 2
- Regulation
- 21 CFR 868.5750
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jeffrey, NH, US
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