OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN— 510(k) K062999
Substantially EquivalentHospira, Inc.
FDA 510(k) clearance K062999 for OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN, Substantially Equivalent on 2006-11-03. Applicant: Hospira, Inc.. Device class: 2.
Clearance details
- Applicant
- Hospira, Inc.
- Product code
- Code DQE
- Device class
- Class 2
- Regulation
- 21 CFR 870.1230
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Lake Forest, IL, US
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More clearances from Hospira, Inc.
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