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Pneumedics, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K904633 SPIROLOOP, MODIFICATIONCCJ1991-03-12 View
510(k) K894667 MODELS PB950 AND PB960 DATALOOP AND SPIROLOOPBTY1989-10-19 View
510(k) K863087 SPIROLOOP-PULMONARY EXERCISE SYSTEMBTY1986-10-27 View
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