PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)— 510(k) K990960
Substantially EquivalentPerimed, Inc.
FDA 510(k) clearance K990960 for PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040), Substantially Equivalent on 1999-09-23. Applicant: Perimed, Inc.. Device class: 2.
Clearance details
- Applicant
- Perimed, Inc.
- Product code
- Code LKD
- Device class
- Class 2
- Regulation
- 21 CFR 868.2480
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Laurel, MD, US
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More clearances from Perimed, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.