Product code MSR— Ophthalmic

FDA has cleared 5 devices under product code MSR between 1997 and 2000, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20001 clearance
• 19983 clearances
• 19971 clearance

• Med-Logics, Inc.2 clearances
• Surgin Surgical Instrumentation, Inc.1 clearance
• Storz Instrument Co.1 clearance
• Hurricane Medical1 clearance

• K993361 — TUBING EXTENSION SETHurricane Medical·2000-01-04
• K983448 — ML UNIVERSAL TUBINGMed-Logics, Inc.·1998-12-18
• K980849 — SURGIN KITSurgin Surgical Instrumentation, Inc.·1998-07-09
• K980100 — STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKStorz Instrument Co.·1998-06-01
• K972522 — ML-DISPOSABLE PAKMed-Logics, Inc.·1997-09-30