Compas
510(k) K021200
Compas is a medical device (FDA Class II; FDA product code BZG, Spirometer, Diagnostic) made by Morgan Scientific, Inc., cleared under FDA 510(k) K021200 on 18 Oct 2002, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK021200 | Date18 Oct 2002 | StatusActive |
Official records
- FDA 510(k) database K021200
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BZG
- Device class
- Class II
- Regulation
- 21 CFR Part 868.1840
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K021200
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| ComPAS 1.10 | 2594 / 1.10 | 00851845007033 | — | On the market |
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