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FDA 510(k)

OPHTHALMIC KNIFE & FORCEPS

K-Number: K864266 · 1986-11-28

ApplicantWestern Medical Products, Inc.
Decision Date1986-11-28
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC KNIFE & FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Western Medical Products, Inc.. It received FDA 510(k) clearance on 1986-11-28 under 510(k) number K864266. 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 OPHTHALMIC KNIFE & FORCEPS?

OPHTHALMIC KNIFE & FORCEPS is a medical device that received FDA 510(k) clearance on 1986-11-28. The listed applicant is Western Medical Products, Inc.. The 510(k) number is K864266.

When did OPHTHALMIC KNIFE & FORCEPS receive FDA 510(k) clearance?

OPHTHALMIC KNIFE & FORCEPS received FDA 510(k) clearance on 1986-11-28, under 510(k) number K864266.

Who is the listed applicant for OPHTHALMIC KNIFE & FORCEPS?

The FDA 510(k) record lists Western Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPHTHALMIC KNIFE & FORCEPS?

The FDA product code for OPHTHALMIC KNIFE & FORCEPS is HNR.

Related Clinical Trials

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.

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Other records listing Western Medical Products, Inc. as applicant

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.

K891487SOFT LENS FOLDING BLOCKK843589TICLIP STERIAL DISPOSABLE

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

View on FDA Database →

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

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