Product code LGH— Orthopedic

FDA has cleared 9 devices under product code LGH between 1982 and 1994, filed by 6 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.

• 19941 clearance
• 19901 clearance
• 19892 clearances
• 19874 clearances
• 19821 clearance

• Martin Medical4 clearances
• Johnson & Johnson Professionals, Inc.1 clearance
• Carapace, Inc.1 clearance
• Buckman Co., Inc.1 clearance
• Bremer Mfg. & Tool Co., Inc.1 clearance
• Black & Decker(Tm)1 clearance

• K932653 — SWISSTEK 2000(TM) CAST REMOVAL SYSTEMCarapace, Inc.·1994-01-28
• K901677 — CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTERBuckman Co., Inc.·1990-04-23
• K893380 — QCR SYSTEM I AND QCR SYSTEM IIBremer Mfg. & Tool Co., Inc.·1989-11-16
• K895861 — DELTA-TECH(TM) CAST REMOVAL SYSTEMJohnson & Johnson Professionals, Inc.·1989-10-19
• K873723 — PLASTER VACUUM, 230V MODEL NO. 4183-161Martin Medical·1987-12-10
• K873721 — PLASTER VACUUM, 115V MODEL NO. 4183-160Martin Medical·1987-12-07
• K873719 — CAST CUTTER, 115V MODEL NO. 4183-106Martin Medical·1987-10-02
• K873720 — CAST CUTTER, 230V MODEL NO. 4183-107Martin Medical·1987-10-02
• K820351 — CAST CUTTER/CAST SAW/INSTRUMENTBlack & Decker(Tm)·1982-03-02