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FDA 510(k)

37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS

K-Number: K851791 · 1985-05-30

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

Device Summary

37-610 TO 37-880 VARIOUS OPHTHAL-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 K851791. 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 37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS?

37-610 TO 37-880 VARIOUS OPHTHAL-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 K851791.

When did 37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS receive FDA 510(k) clearance?

37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS received FDA 510(k) clearance on 1985-05-30, under 510(k) number K851791.

Who is the listed applicant for 37-610 TO 37-880 VARIOUS OPHTHAL-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 37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS?

The FDA product code for 37-610 TO 37-880 VARIOUS OPHTHAL-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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