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Laser Industries, Ltd.

Mchenry, IL, US

Laser Industries , Ltd. appears in FDA device records in Mchenry, IL. FDA records list 20 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
20
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 20 510(k) clearances for Laser Industries, Ltd. between 1978 and 1994. The busiest year on record is 1983, with 4. The most recent is 1994, with 1.

Clearances by year, as a table
510(k) clearance decisions for Laser Industries, Ltd., by decision year
YearClearances
19781
19792
19802
19823
19834
19844
19852
19891
19941
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K933362SHARPLAN CO2 SURGICAL LASERGEXSubstantially Equivalent
K894765SHARPLAN SMOKE EVACUATION UNIT, MODEL 100FYDSubstantially Equivalent
K850633SHARPLAN MODEL 1060 CO/2 SURGICAL LASERGEXSubstantially Equivalent
K850628SHARPLAN 1040 CO/2 SURGICAL LASERGEXSubstantially Equivalent
K842997LASER RECTOSCOPE SET 784FDCSubstantially Equivalent
K832550SHARPLAN #734 LASER SURGICAL UNITGEXSubstantially Equivalent
K832551SHARPLAN #745 LASER SURG. UNITSubstantially Equivalent
K832316OPHTHALMIC ARGON LASER #700AHQFSubstantially Equivalent
K837573SHARPLAN LASER POSITIONING SYSTEMSubstantially Equivalent
K837342SHARPLAN 721 CO2 SURGICAL LASERSubstantially Equivalent
K837081MICROSCAN 771 MANIPULATORSubstantially Equivalent
K828056MODEL 716 MICROMANIPULATORSubstantially Equivalent
K828194LASER LAPAROSCOPESubstantially Equivalent
K827607MODEL 712 MICROMANIPULATORSubstantially Equivalent
K820101SHARPLAN 720 CO2 SURGICAL LASERGEXSubstantially Equivalent
K801624SHARPLAN 723 CO2 LASER SURGICAL SYSTEMGEXSubstantially Equivalent
K792418SHARPLAN 743, CO2 LASER SURGICAL SYSTEMGEXSubstantially Equivalent
K790526LIO-714 OPACITYMETERHJLSubstantially Equivalent
K782030LASER SYSTEM, SHARPLAN 791/HE, CO2GEXSubstantially Equivalent
K780585SURGICAL LASERGEXSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain