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

COHERENT MARIE ARGON PHOTOCOAGULATOR

K Number: K893709 · Decision Jun 15, 1989
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
27
Review Days
28

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Basic Information

Device Name
COHERENT MARIE ARGON PHOTOCOAGULATOR
K Number
K893709
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Coherent Medical Group
Date Received
May 18, 1989
Decision Date
June 15, 1989
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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K923575 COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS
K932468 NOVUS MULTIWAVELENGTH
K930981 ACCULITE(TM) OTOPROBE
K914136 COHERENT VERSAPULSE(TM) 2.1XE/2.1L HOLMI SURG LASE
K914991 VERSAPULSE(TM) TWOPOINTONE/XE HOLMIUM SURG LASERS
K913127 COHERENT NOVUS 3000 ARGON PHOTOCOAGULATOR
K910037 COHERENT HOLMIUM:YAG SURGICAL LASER
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