Product code FSQ— General, Plastic Surgery

FDA has cleared 7 devices under product code FSQ between 1981 and 1993, 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.

• 19933 clearances
• 19921 clearance
• 19813 clearances

• Medical Products Development, Inc.3 clearances
• Alm Surgical Equipment, Inc.2 clearances
• Midmark Corp.1 clearance
• Aaron Medical Industries1 clearance

• K930686 — MIDMARK SURGICAL LIGHTING SYSTEMSMidmark Corp.·1993-07-30
• K932139 — LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFTAaron Medical Industries·1993-07-30
• K922409 — ALM ILLUMINATOR SERIES LIGHT SYSTEMAlm Surgical Equipment, Inc.·1993-01-12
• K921848 — BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHTAlm Surgical Equipment, Inc.·1992-10-01
• K803067 — SURG-FLEX 10 LIGHTMedical Products Development, Inc.·1981-02-26
• K810018 — SURG-FLEX 5 SURGICAL LIGHTMedical Products Development, Inc.·1981-01-23
• K810019 — SURG-FLEX 15 SURGICAL LIGHTMedical Products Development, Inc.·1981-01-23