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Pneumedics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K904633SPIROLOOP, MODIFICATIONMarch 12, 1991
K894667MODELS PB950 AND PB960 DATALOOP AND SPIROLOOPOctober 19, 1989
K863087SPIROLOOP-PULMONARY EXERCISE SYSTEMOctober 27, 1986