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FDA 510(k)

THORNTON TITANIUM FORCEPS (VARIOUS TYPES)

K-Number: K863992 · 1986-10-31

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

Device Summary

THORNTON TITANIUM FORCEPS (VARIOUS TYPES) is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863992. 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 THORNTON TITANIUM FORCEPS (VARIOUS TYPES)?

THORNTON TITANIUM FORCEPS (VARIOUS TYPES) is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K863992.

When did THORNTON TITANIUM FORCEPS (VARIOUS TYPES) receive FDA 510(k) clearance?

THORNTON TITANIUM FORCEPS (VARIOUS TYPES) received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863992.

Who is the listed applicant for THORNTON TITANIUM FORCEPS (VARIOUS TYPES)?

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

What is the FDA product code for THORNTON TITANIUM FORCEPS (VARIOUS TYPES)?

The FDA product code for THORNTON TITANIUM FORCEPS (VARIOUS TYPES) is HNR.

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Other records listing Keeler Instruments, Inc. as applicant

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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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