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FDA 510(k)

CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)

K-Number: K962255 · 1996-09-11

ApplicantClarus Medical Systems, Inc.
Decision Date1996-09-11
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) is the device name listed in this FDA 510(k) record. The listed applicant is Clarus Medical Systems, Inc.. It received FDA 510(k) clearance on 1996-09-11 under 510(k) number K962255. 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 CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)?

CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is Clarus Medical Systems, Inc.. The 510(k) number is K962255.

When did CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) receive FDA 510(k) clearance?

CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) received FDA 510(k) clearance on 1996-09-11, under 510(k) number K962255.

Who is the listed applicant for CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)?

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

What is the FDA product code for CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)?

The FDA product code for CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) is EOB.

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Other records listing Clarus Medical Systems, 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.

K980588CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000K974579PERCSCOPE MODEL 2600K971584CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)K971455CLARUS MODEL 5197 SIGHTLITEK960915CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXXK955598CLARUS SPINEPEN MODEL 2126

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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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