FDA 510(k) FDA class 1 Substantially Equivalent 🇫🇷 France

ANESTHESIOMETER

K Number: K851557 · Decision May 30, 1985
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
1
Applicant Total
3
Review Days
44

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Basic Information

Device Name
ANESTHESIOMETER
K Number
K851557
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1040
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Luneau SA
Date Received
April 16, 1985
Decision Date
May 30, 1985
Product Code
HJC
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
HJC Esthesiometer, Ocular

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Other Clearances by Luneau SA

K Number Device Name
K023838 LUNEAU STERILE TONOMETER SEPARATION PRISMS
K022413 LUNEAU 3 MIRROR LENS