Atlas FDA

HOS

9 FDA 510(k) clearances · Product code

79 daysmedian time to decision
273 days90th percentile
9clearances measured

FDA profile

Official device name
Projector, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.1680
Medical specialty
Ophthalmic
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RecordFirmDate
WIRELESS CHART PROJECTOR,HCP-W 721 (K936200)Canon USA, Inc.1994-09-28
MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE (K930443)Marco Ophthalmic, Inc.1993-07-06
BURTON PROJECTOR HEAD - MODEL 6000-H (K924784)R.H. Burton Co.1993-04-05
OPHTHALMIC PROJECTOR (K921214)Luneau Ophtalmologie SA1992-06-11
WOODLYN OPHTHALMIC PROJECTOR (K890992)Woodlyn, Inc.1989-05-17
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR (K862519)Bausch & Lomb, Inc.1986-07-23
MILLER/NADLER GLARE TESTER (K812706)Mosebach Electric & Supply1981-11-16
ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ (K811180)American Optical Corp.1981-05-15
PROJECTOR, ACCU-CHART ACUITY (K781658)Bausch & Lomb, Inc.1978-10-17

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Every clearance here is in the API, with alerts when new ones post.