Product code HRR— Orthopedic

FDA has cleared 8 devices under product code HRR between 1980 and 1989, filed by 5 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.

• 19893 clearances
• 19872 clearances
• 19851 clearance
• 19841 clearance
• 19801 clearance

• Kinetic Medical Products3 clearances
• Arthropedics, Inc.2 clearances
• Edward Weck, Inc.1 clearance
• Artiberia1 clearance
• All-Hands Medical Supply, Inc.1 clearance

• K890212 — MICROSURGICAL SCISSORSKinetic Medical Products·1989-01-27
• K890225 — SURGICAL SCISSORSKinetic Medical Products·1989-01-27
• K890261 — TRIGEMINAL SCISSORSKinetic Medical Products·1989-01-27
• K873501 — SCISSOR, LEFTArthropedics, Inc.·1987-11-02
• K873502 — SCISSOR, RIGHTArthropedics, Inc.·1987-11-02
• K851800 — 69-100 TO 69-114 VARIOUS CUTICLE SCISSORSArtiberia·1985-06-20
• K842953 — ALL-HANDS MEDICAL SUPPLY SUTURE REMOVALAll-Hands Medical Supply, Inc.·1984-08-21
• K800721 — GENERAL UTILITY SURG. SCISSORS #460180-Edward Weck, Inc.·1980-05-08