KONTRON CUTANEOUS PCO2 MONITOR
FDA premarket approval P810037/S002 · decided 1982-12-22
Approval details
- PMA number
- P810037
- Supplement
- S002
- Trade name
- KONTRON CUTANEOUS PCO2 MONITOR
- Generic name
- MONITOR, CARBON-DIOXIDE, CUTANEOUS
- Applicant
- Kontron Cardiovascular
- Date received
- 1982-09-14
- Decision date
- 1982-12-22
- Days to decision
- 99 days
- Decision code
- APPR
- Product code
- LKD
- Advisory committee
- Anesthesiology
- Expedited review
- No
- Location
- Everett, MA
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