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FDA 510(k)

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS

K-Number: K851792 · 1985-05-30

ApplicantArtiberia
Decision Date1985-05-30
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K851792. 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 37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS?

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is Artiberia. The 510(k) number is K851792.

When did 37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS receive FDA 510(k) clearance?

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS received FDA 510(k) clearance on 1985-05-30, under 510(k) number K851792.

Who is the listed applicant for 37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS?

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

What is the FDA product code for 37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS?

The FDA product code for 37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS is HNR.

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Other records listing Artiberia 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.

K8517451-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON BK85178627-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

View all 79 devices →

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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