FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PHOTRON VISUAL FIELD ANALYZER

K Number: K860642 · Decision Apr 15, 1986
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
10
Review Days
54

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Basic Information

Device Name
PHOTRON VISUAL FIELD ANALYZER
K Number
K860642
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1810
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Biosan Laboratories, Inc.
Date Received
February 20, 1986
Decision Date
April 15, 1986
Product Code
HOM
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
HOM Screen, Tangent, Ac-Powered (Campimeter)

Other Clearances by Biosan Laboratories, Inc.

K Number Device Name
K853812 PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)
K832763 TOBRAMYCIN REAGENT
K833193 RADIOIMMUNOASSAY, THYROID STIMU. HORMONE
K834023 BIO-SCIENCE LABORATORIES T4 REAGENT
K833318 NORMAL GOAT SERUM
K833192 NORMAL URINE CONTROL
K833191 ABNORMAL URINE CONTROL
K833320 AMBERLITE CG50 RESIN, 100-200 MESH
K833319 BIO-REX 70 RESIN 100-200 MESH PH6.2