Find 510K Clearence requests from to with applicant of device name containing

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510(k) Number/Type
Applicant
Device
Advisory Committe
Date Received
Decision Date
More Info
K902779 S & W MEDICO TEKNIK MODIFICATION TYPE 9266 SA02 SYSTEM ATHENA Cardiovascular 1990-06-06 1990-09-27
K901989 CROW RIVER INDUSTRIES, INC. GRAVITY DOWN WHEELCHAIR LIFT Physical Medicine 1990-05-02 1990-05-24
K901786 LASER PERIPHERALS LLC. LASEGUIDE CAT # CLF-600D & CLF-1000D General, Plastic Surgery 1990-04-18 1990-06-27
K901265 COULTER CORP. COULTER MAGNESIUM REAGENT Clinical Chemistry 1990-03-16 1990-03-29
K901198 CARTER PRODUCTS TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED Obstetrics/Gynecology 1990-03-12 1990-04-16
K901089 MARQUETTE MEDICAL, INC. LOW VOLUME TRIFURCATED IV EXTENSION SET General Hospital 1990-03-07 1990-10-04
K900756 INTERVENTIONAL THERAPEUTICS CORP. ITC INTRODUCER CATHETER Cardiovascular 1990-02-16 1990-08-08
K900548 SHILEY, INC. SHILEY PHONATION VALVE Anesthesiology 1990-02-05 1990-04-23
K861307 ANAGO, INC. DISPOSABLE NEEDLE COUNTER General Hospital 1986-04-08 1986-05-02
K861322 RESEARCH MEDICAL, INC. RMI POROUS VENT PLUG Cardiovascular 1986-04-08 1986-05-30

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