Techna Vision, Inc.Electric Table

FDA 510(k) K853744 · Techna Vision

Substantially Equivalent

510(k) numberK853744

Submission

Device name
Techna Vision, Inc.Electric Table
Applicant
Techna Vision
Santee, CA, US
Received
September 6, 1985
Decision date
October 17, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HRJ – Table, Instrument, Powered, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4855
Specialty
Ophthalmic

Other 510(k)s with product code HRJ

510(k)DeviceApplicantDecision
K930447Marco H and TS-1 Instrument TablesHRJ · Traditional Marco Ophthalmic, Inc.07/06/1993SE
K922242910T Montorized Instrument TableHRJ · Traditional R.H. Burton Co.09/30/1992SE
K912134TBD, Lens Measuring DeviceHRJ · Traditional Alcon Laboratories07/25/1991SE
K853359Reliance 1379HRJ · Traditional Dentsply Intl.09/24/1985SE
K841760Woodlyn Classic Instrument StandHRJ · Traditional Woodlyn, Inc.06/19/1984SE
K833820Machemer/Tano RotatingHRJ · Traditional Optical Micro Systems, Inc.01/04/1984SE

More from Optical Micro Systems, Inc.

510(k)DeviceDecision
K862578Techna Vision Casting ResinHQG · Traditional 07/23/1986SE
K853290Techna Vision Auto-PerimeterHPT · Traditional 11/12/1985SE
K853743Techna Vision, Inc. Electric ChairHME · Traditional 10/17/1985SE

Questions and answers

When was Techna Vision, Inc.Electric Table cleared by the FDA?

Techna Vision, Inc.Electric Table (K853744) received a 510(k) decision of Substantially Equivalent on October 17, 1985, 41 days after the submission was received.

What is the product code of K853744?

The FDA product code is HRJ – Table, Instrument, Powered, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4855.