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FDA 510(k)

IOL IMPLANTATION FORCEPS

K-Number: K883197 · 1988-08-22

ApplicantD & D Surgical
Decision Date1988-08-22
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IOL IMPLANTATION FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is D & D Surgical. It received FDA 510(k) clearance on 1988-08-22 under 510(k) number K883197. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IOL IMPLANTATION FORCEPS?

IOL IMPLANTATION FORCEPS is a medical device that received FDA 510(k) clearance on 1988-08-22. The listed applicant is D & D Surgical. The 510(k) number is K883197.

When did IOL IMPLANTATION FORCEPS receive FDA 510(k) clearance?

IOL IMPLANTATION FORCEPS received FDA 510(k) clearance on 1988-08-22, under 510(k) number K883197.

Who is the listed applicant for IOL IMPLANTATION FORCEPS?

The FDA 510(k) record lists D & D Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IOL IMPLANTATION FORCEPS?

The FDA product code for IOL IMPLANTATION FORCEPS is HNR.

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Related Devices (Code: HNR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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