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

FOCOMETER

K Number: K944402 · Decision Nov 22, 1994
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
46
Applicant Total
12
Review Days
71

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Basic Information

Device Name
FOCOMETER
K Number
K944402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lacrimedics, Inc.
Date Received
September 12, 1994
Decision Date
November 22, 1994
Product Code
HLJ
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
HLJ Ophthalmoscope, Battery-Powered

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Other Clearances by Lacrimedics, Inc.

K Number Device Name
K161673 LacriPro Punctum Plug
K140026 COLLASYN PLUG FOR THE LACRIMAL EFFICIENCY TEST
K030300 OPAQUE HERRICK LACRIMAL PLUG
K021831 OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPB
K001737 OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM
K963708 HERRICK ULTIMATE PUNCTUM PLUG
K963501 HERRICK ULTIMATE PUNCTUM PLUG
K896175 HERRICK LACRIMAL PLUG TM.
K895342 COLLAGEN IMPLANTS FOR THE LACRIMAL EFFICIENCY TEST
K890714 LACRIMAL EFFICIENCY TEST (TM)
Search all 12 clearances from Lacrimedics, Inc. →