SYRINGEFILTER— 510(k) K960928
Substantially EquivalentArbor Technologies, Inc.
FDA 510(k) clearance K960928 for SYRINGEFILTER, Substantially Equivalent on 1997-04-04. Applicant: Arbor Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Arbor Technologies, Inc.
- Product code
- Code BSN
- Device class
- Class 2
- Regulation
- 21 CFR 868.5130
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ann Arbor, MI, US
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