Atlas FDA

QUANTUM 412

FDA 510(k) clearance K844570 · decided 1984-12-05

Clearance details

K-number
K844570
Device name
QUANTUM 412
Applicant
Keta Corp.
Decision
Substantially Equivalent
Date received
1984-11-23
Decision date
1984-12-05
Days to decision
12 days
Clearance type
Traditional
Product code
HPT
Device class
1
Regulation number
886.1605
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Danvers, MA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MAIA, MODEL 1 (K092187)Centervue S.P.A.2010-05-27
GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIES (K093213)Carl Zeiss Meditec, Inc.2010-03-12
FORESEE HOME (K091579)Notal Vision , Ltd.2009-12-23
TRUEFIELD ANALYZER (K063310)Seeing Machines Limited2007-08-02
THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP) (K050350)Notal Vision, Inc.2005-04-29
NOVAVISION, MODEL 2.0 (K023623)Novavision, Inc.2003-04-22
KASHA VISUAL FIELD SYSTEM (K971156)Kasha Software, Inc.1997-05-28
AUTOMATIC VISUAL FIELD PLOTTER AP-125 (K961090)Kowa Optimed, Inc.1996-06-17
HUMPHREY FIELD ANALYZER (HFA II) (K954167)Carl Zeiss, Inc.1995-11-24
FIELD TREND (K954037)Synemed, Inc.1995-11-17
MS-30 AUTOMATIC PERIMETER (K943234)Marco Ophthalmic, Inc.1994-07-27
OPTICOM M600 (K932258)Clement Clarke, Inc.1994-07-25

Recalls involving this device

No recalls on record reference this clearance.