CAPIOX LEVEL ALARM— 510(k) K915337
Substantially EquivalentTerumo Medical Corp.
FDA 510(k) clearance K915337 for CAPIOX LEVEL ALARM, Substantially Equivalent on 1992-02-21. Applicant: Terumo Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Terumo Medical Corp.
- Product code
- Code DTW
- Device class
- Class 2
- Regulation
- 21 CFR 870.4340
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elkton, MD, US
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More clearances from Terumo Medical Corp.
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