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

KEELER MULTILASE 3000

K Number: K942180 · Decision Nov 22, 1994
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
60
Review Days
202

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Basic Information

Device Name
KEELER MULTILASE 3000
K Number
K942180
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Keeler Instruments, Inc.
Date Received
May 4, 1994
Decision Date
November 22, 1994
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 Keeler Instruments, Inc.

K Number Device Name
K181143 Keeler TonoCare Tonometer
K112093 CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER
K093298 PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000
K100500 PSL CLASSIC SLIT LAMP
K062412 CRYOMATIC
K060822 VANTAGE INDIRECT OPHTHALMOSCOPE
K032087 KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004
K992954 KEELER CRYO MASTER & PROBES
K990257 KEELER PULSAIR 3000 NON CONTACT TONOMETER
K973064 KEELER TEARSCOPE-PLUS
Search all 60 clearances from Keeler Instruments, Inc. →