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

CERALAS DIODE LASER SYSTEM (CERALAS D2)

K Number: K964751 · Decision Feb 21, 1997
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
30
Review Days
87

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Basic Information

Device Name
CERALAS DIODE LASER SYSTEM (CERALAS D2)
K Number
K964751
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ceram Optec, Inc.
Date Received
November 26, 1996
Decision Date
February 21, 1997
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 Ceram Optec, Inc.

K Number Device Name
K002296 CERALAS G15 532NM FREQUENCY DOUBLED ND:YAG LASER, MODEL G1-G15
K001975 CERALAS D10 810NM LASER, MODEL CERALAS D10-60
K993911 CERALAS D DIODE LASER SYSTEM, MODEL D15, D25,D50
K993828 CERALAS D10 810NM DIODE LASER
K993002 CERALAS D 980NM DIODE LASER SYSTEM, MODEL D15
K992773 CERALAS D10 810NM DIODE LASER
K991891 CERALAS DIODE LASER SYSTEM, MODEL CERALAS D15
K983950 CERALAS DIODE LASER SYSTEM (MODEL H)
K983058 CERALAS D LASER SYSTEM, MODEL # CERALAS D15
K980389 MEGABEAM REUSABLE FIBER OPTIC HANDPIECE AND NEEDLES
Search all 30 clearances from Ceram Optec, Inc. →