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FDA 510(k)

CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE

K-Number: K924554 · 1993-02-25

ApplicantClarus Medical Systems, Inc.
Decision Date1993-02-25
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE 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 1993-02-25 under 510(k) number K924554. The device is classified under product code LYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE?

CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1993-02-25. The listed applicant is Clarus Medical Systems, Inc.. The 510(k) number is K924554.

When did CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE receive FDA 510(k) clearance?

CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE received FDA 510(k) clearance on 1993-02-25, under 510(k) number K924554.

Who is the listed applicant for CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE?

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 SERIRS 2200 SEMI-RIGID ENDOSCOPE?

The FDA product code for CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE is LYK.

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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-XXXK962255CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)

View all 22 devices →

Related Devices (Code: LYK)

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.

K253842Vena MicroAngioscope™ SystemVena Medical Holdings CorpK251767Vena MicroAngioscope™ SystemVena Medical Holdings CorpK062340CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEMCardio-Optics, Inc.K050808CORONARY SINUS ACCESS KIT, MODEL KCS8F-01Cardio-Optics, Inc.K011793KSEA FIBERSCOPEKARL STORZ Endoscopy-America, Inc.K012724SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273Smith & Nephew, 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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