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FDA 510(k)

JARIT RECOMMENDED SINUS INSTRUMENTS

K-Number: K941565 · 1994-05-16

ApplicantJ. Jamner Surgical Instruments, Inc.
Decision Date1994-05-16
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

JARIT RECOMMENDED SINUS INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is J. Jamner Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K941565. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JARIT RECOMMENDED SINUS INSTRUMENTS?

JARIT RECOMMENDED SINUS INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is J. Jamner Surgical Instruments, Inc.. The 510(k) number is K941565.

When did JARIT RECOMMENDED SINUS INSTRUMENTS receive FDA 510(k) clearance?

JARIT RECOMMENDED SINUS INSTRUMENTS received FDA 510(k) clearance on 1994-05-16, under 510(k) number K941565.

Who is the listed applicant for JARIT RECOMMENDED SINUS INSTRUMENTS?

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

What is the FDA product code for JARIT RECOMMENDED SINUS INSTRUMENTS?

The FDA product code for JARIT RECOMMENDED SINUS INSTRUMENTS is EOB.

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Other records listing J. Jamner Surgical Instruments, 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.

K082349JARIT HULKA UTERINE TENACULUM FORCEPSK944670JARIT RECOMMENDED SINUS INSTRUMENTSK944870JARIT ENDOSCOPES, MODELS 600-600; 600-630; 600-650; AND 600-680K932456JARIT SURGICAL INSTRUMENTSK933728JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-334, 615-335, 615-338, 615-339K931928JARIT SURGICAL INSTRUMENTS

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Related Devices (Code: EOB)

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.

K254299CLEARVISION Irrigation Sheath 0° (7241AS); CLEARVISION Irrigation Sheath 30° (7241BS); CLEARVISION Irrigation Sheath 45° (7241FS)Karl Storz SE & CO. KGK261544Hydro Irrigation SystemStryker InstrumentsK254133ENTity USB Videoscope SystemOptim, LLCK253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)Zhuhai Wesee Meditech Co., Ltd.K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241DOlympus Medical Systems CorporationK241731Outlook Surgical Versa One System (8900139)Resnent, LLC

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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