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

PASCAL STREAMLINE PHOTOCOAGULATOR

K Number: K092621 · Decision Sep 25, 2009
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
6
Review Days
30

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Basic Information

Device Name
PASCAL STREAMLINE PHOTOCOAGULATOR
K Number
K092621
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Topcon Medical Laser Systems, Inc.
Date Received
August 26, 2009
Decision Date
September 25, 2009
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 Topcon Medical Laser Systems, Inc.

K Number Device Name
K180402 PSLT with PASCAL Synthesis, PSLT with PASCAL Synthesis TwinStar
K171488 PSLT for PASCAL Streamline
K123542 PASCAL SYNTHESIS (532NM/577NM) OPTHALMIC LASER
K111108 PASCAL STREAMLINE 577 (WITH ACCESSORIES)
K043486 PASCAL PHOTOCOAGULATOR, PRODUCT-PASCAL-01