Warren E. Collins, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K925459 | GS-MODULAR (GOLD STANDARD - MODULAR) | February 4, 1994 |
| K912946 | COLLINS DIGITAL PULMONARY MANOMETER | January 15, 1992 |
| K871151 | THE SPIRA ELEKTRO 2 | May 15, 1987 |
| K861227 | COLLINS PNEUMOTACH PFT SYSTEM | June 5, 1986 |
| K852102 | COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM | July 31, 1985 |
| K831780 | METABOLIC EXERCISE TESTING SYSTEM | September 12, 1983 |
| K831777 | COLLINS DS | August 31, 1983 |
| K831778 | RS-RESIDUAL VOLUME SYSTEM | August 31, 1983 |
| K831779 | COLLINS EAGLE II | August 26, 1983 |
| K803053 | APEXLINE OF PULMONARY FUNCT. INSTRUM. | December 22, 1980 |
| K803069 | SHELL KRATON THERMO-PLASTIC RUBBER COMP. | December 22, 1980 |
| K781889 | COLLINS PEDALMATE 2 | November 22, 1978 |
| K780584 | PULMONARY FUNCTION TESTER | May 16, 1978 |
| K780328 | PULMONARY FUNCTION TESTER, COMPUTERIZED | March 14, 1978 |