ATMOS C 051 Thorax (317.0200.0); Secretion canister 800ml (317.1300.0); Hose system (312.1177.0); Hose system with connector small (312.1206.0); Hose system with connector medium (312.1207.0); Hose system with connector large (312.1208.0); Hose system with Y-connector medium (312.1209.0); Hose system with Y-connector large (312.1210.0); Universal bracket for ATMOS C 051 Thorax (316.0200.0); Bracket for ATMOS C 051 Thorax - Standard rail (317.1160.0); Charger Storage for bracket ATMOS C
K241799 is the FDA 510(k) clearance record for ATMOS C 051 Thorax (317.0200.0); Secretion canister 800ml (317.1300.0); Hose system (312.1177.0); Hose system with connector small (312.1206.0); Hose system with connector medium (312.1207.0); Hose system with connector large (312.1208.0); Hose system with Y-connector medium (312.1209.0); Hose system with Y-connector large (312.1210.0); Universal bracket for ATMOS C 051 Thorax (316.0200.0); Bracket for ATMOS C 051 Thorax - Standard rail (317.1160.0); Charger Storage for bracket ATMOS C, a class II device, cleared for Atmos Medizintechnik GmbH & Co. KG on under FDA product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). FDA records list 2 510(k) clearances for Atmos Medizintechnik GmbH & Co. KG, from to . As of , FDA records show no recalls naming K241799.
Clearance record
- Decision date
- Received
- (259 days to decision)
- Product code
- BTA Pump, Portable, Aspiration (Manual Or Powered)
- Regulation
- 21 CFR 878.4780
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Atmos Medizintechnik GmbH & Co. KG Ludwig-Kegel-Str. 16, Lenzkirch, DE
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code BTA
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 4 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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