K013856Substantially Equivalent
Pmh 1000 Heated Humidifier
Pegasus Research Corp., Santa Ana CA / Traditional, Substantially Equivalent
K013856 is the FDA 510(k) clearance record for PMH 1000 HEATED HUMIDIFIER, a class II device, cleared for Pegasus Research Corp. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 12 510(k) clearances for Pegasus Research Corp., from to . As of , FDA records show no recalls naming K013856.
Clearance record
- Decision date
- Received
- (472 days to decision)
- Product code
- BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
- Regulation
- 21 CFR 868.5450
- Device class
- Class II
- Review panel
- Anesthesiology
- Applicant
- Pegasus Research Corp. 1714 S. Lyon St., Santa Ana CA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code BTT
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 2 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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