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

MARCO LM-770 DIGITAL PROJECTION LENSMETER

K Number: K930445 · Decision Jun 21, 1993
Classifications
1
FEI Numbers
64
Registration Numbers
65
Same Product Code
15
Applicant Total
15
Review Days
146

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MARCO LM-770 DIGITAL PROJECTION LENSMETER
K Number
K930445
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1425
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Marco Ophthalmic, Inc.
Date Received
January 26, 1993
Decision Date
June 21, 1993
Product Code
HLM
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
HLM Instrument, Measuring, Lens, Ac-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HLM), ordered by most recent decision date.

View all

Other Clearances by Marco Ophthalmic, Inc.

K Number Device Name
K943234 MS-30 AUTOMATIC PERIMETER
K930437 MARCO STANDARD RADIUSGAUGES
K930444 MARCO STANDARD KERATOMETERS
K930442 MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPS
K930438 MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPS
K930439 MARCO SURGISCOPE OPERATION MICROSCOPES
K930443 MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE
K930449 MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR
K930446 MARCO TRIAL SETS
K930441 MARCO STANDARD LENSMETERS 101,201
Search all 15 clearances from Marco Ophthalmic, Inc. →