Shure Grip Tying Forceps

FDA 510(k) K844129 · Mentor O & O, Inc.

Substantially Equivalent

510(k) numberK844129

Submission

Device name
Shure Grip Tying Forceps
Applicant
Mentor O & O, Inc.
Hingham, MA, US
Received
October 23, 1984
Decision date
November 21, 1984
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

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Questions and answers

When was Shure Grip Tying Forceps cleared by the FDA?

Shure Grip Tying Forceps (K844129) received a 510(k) decision of Substantially Equivalent on November 21, 1984, 29 days after the submission was received.

What is the product code of K844129?

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