BENTLEY THEROMODILUTION CATHETER #BTD-7F— 510(k) K802133
Substantially EquivalentBentley Laboratories, Inc.
FDA 510(k) clearance K802133 for BENTLEY THEROMODILUTION CATHETER #BTD-7F, Substantially Equivalent on 1980-09-26. Applicant: Bentley Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Bentley Laboratories, Inc.
- Product code
- Code KRB
- Device class
- Class 2
- Regulation
- 21 CFR 870.1915
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Bentley Laboratories, Inc.
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