Product code IPR— Physical Medicine

FDA has cleared 4 devices under product code IPR between 1977 and 1982, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19821 clearance
• 19801 clearance
• 19791 clearance
• 19771 clearance

• Maddak, Inc.2 clearances
• Manuco Manufacturing Co., Inc.1 clearance
• Husa Folding Crutch Co., Inc.1 clearance

• K821403 — LIGHT WEIGHT ALUMINUM CRUTCHESManuco Manufacturing Co., Inc.·1982-06-21
• K800237 — FOLDING CRUTCHHusa Folding Crutch Co., Inc.·1980-02-22
• K790557 — CRUTCHMaddak, Inc.·1979-04-03
• K770146 — SWIVEL HEAD ADJUSTABLE CRUTCHMaddak, Inc.·1977-01-28