FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR

K Number: K070776 · Decision Apr 24, 2007
Classifications
1
FEI Numbers
61
Registration Numbers
62
Same Product Code
176
Applicant Total
21
Review Days
34

Basic Information

Device Name
SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR
K Number
K070776
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
QUANTEL MEDICAL
Date Received
March 21, 2007
Decision Date
April 24, 2007
Product Code
HQF
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HQF Laser, Ophthalmic

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Other Clearances by QUANTEL MEDICAL

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K140336 OPTIMUS FUSION: SLT, YAG AND YAG/SLT
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K100678 SUPRA SCAN DELIVERY SYSTEM
K091581 SUPRA 577.Y LASER
K081946 SUPRA TWIN OPHTHALMIC LASER PHOTOCOAGULATOR
K051851 AVISO OPHTHALMIC ULTRASOUND SYSTEM
K043613 Q-SWITCHED ND:YAG OPHTALMIC LASER (WITH SLIT LAMP), MODEL OPTIMIS II
K043236 FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA
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