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FDA 510(k)

PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS

K-Number: K864003 · 1986-10-31

ApplicantAllergan, Inc.
Decision Date1986-10-31
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K864003. 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 PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS?

PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Allergan, Inc.. The 510(k) number is K864003.

When did PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS receive FDA 510(k) clearance?

PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS received FDA 510(k) clearance on 1986-10-31, under 510(k) number K864003.

Who is the listed applicant for PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS?

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

What is the FDA product code for PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS?

The FDA product code for PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS is HNR.

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Other records listing Allergan, 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.

K190674REFRESH RELIEVA For CONTACTSK161457XEN Glaucoma Treatment SystemK083812REFRESH OPTIVE LENS COMFORT REWETTING DROPSK051852SINGLE AMPLIFIER FOR BOTOXK014202COMPLETE BRAND MULTI-PURPOSE SOLUTIONK013479COMPLETE BRAND MULTI-PURPOSE SOLUTION

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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

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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