Ascon Surgical Instruments

FDA 510(k) K852057 · Ascon Medical Instruments, Ltd.

Substantially Equivalent

510(k) numberK852057

Submission

Device name
Ascon Surgical Instruments
Applicant
Ascon Medical Instruments, Ltd.
Westmont, IL, US
Received
May 9, 1985
Decision date
June 27, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HNR – Forceps, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4350
Specialty
Ophthalmic

Other 510(k)s with product code HNR

510(k)DeviceApplicantDecision
K022835Stephens Disposable ForcepsHNR · Traditional Stephens Instruments11/01/2002SE
K895434Alcon Folding ForcepsHNR · Traditional Alcon Laboratories12/04/1989SE
K891487Soft Lens Folding BlockHNR · Traditional Western Medical Products, Inc.08/15/1989SE
K893199Phaco-Injector(Tm) Intraocular Lens Implant InstrHNR · Traditional Allergan Medical Optics06/16/1989SE
K885230Mcdonald Folding ForcepsHNR · Traditional Alcon Laboratories05/17/1989SE
K881049Bradbury Intraocular Retinal Kit Cat #200HNR · Traditional Microline Pentax, Inc.09/12/1988SE
K883197Iol Implantation ForcepsHNR · Traditional D & D Surgical08/22/1988SE
K880274Advanced Surgical Products Scleral Plug ForcepsHNR · Traditional Advanced Surgical Products, Inc.02/05/1988SE
K864266Ophthalmic Knife & ForcepsHNR · Traditional Western Medical Products, Inc.11/28/1986SE
K864183Ophthalmic Surgical InstrumentsHNR · Traditional Techno Ophthalmics Intl.11/28/1986SE

More from Techno Ophthalmics Intl.

510(k)DeviceDecision
K852054Contact Lens Loupe, Inspetion LoupeHLN · Traditional 09/05/1985SE
K852055Ascon Ophthalmic SpongeHOZ · Traditional 09/04/1985SE
K852548Atl 225 MW Trail Lens SetHPA · Traditional 07/31/1985SE
K852126Atf 101 Trail FrameHPA · Traditional 06/05/1985SE
K852056Acc Cross CylindersHPC · Traditional 06/05/1985SE

Questions and answers

When was Ascon Surgical Instruments cleared by the FDA?

Ascon Surgical Instruments (K852057) received a 510(k) decision of Substantially Equivalent on June 27, 1985, 49 days after the submission was received.

What is the product code of K852057?

The FDA product code is HNR – Forceps, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4350.