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FDA 510(k)

CLARUS ENDOSCOPIC BALL PROBE

K-Number: K926048 · 1993-04-07

ApplicantClarus Medical Systems, Inc.
Decision Date1993-04-07
Product CodeGZX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CLARUS ENDOSCOPIC BALL PROBE 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 1993-04-07 under 510(k) number K926048. The device is classified under product code GZX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLARUS ENDOSCOPIC BALL PROBE?

CLARUS ENDOSCOPIC BALL PROBE is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Clarus Medical Systems, Inc.. The 510(k) number is K926048.

When did CLARUS ENDOSCOPIC BALL PROBE receive FDA 510(k) clearance?

CLARUS ENDOSCOPIC BALL PROBE received FDA 510(k) clearance on 1993-04-07, under 510(k) number K926048.

Who is the listed applicant for CLARUS ENDOSCOPIC BALL PROBE?

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 ENDOSCOPIC BALL PROBE?

The FDA product code for CLARUS ENDOSCOPIC BALL PROBE is GZX.

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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)

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Related Devices (Code: GZX)

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.

K932169MICROSURGICAL INSTRUMENTSAmerican Russian Medical Services, Inc.K911932J105 JAMES SURGICAL SYSTEM I/A PACKO.R. Specialties, Inc.K890216MICROSURGICAL KERATOMEKinetic Medical ProductsK873933RANGE OF NEUROSURGICAL INSTRUMENTS IN TITANIUMDowns Surgical , Ltd.K873934RANGE OF CROCODILE ACTION INSTRUMENTSDowns Surgical , Ltd.K862971MICRA MICROSURGICAL INSTRUMENTSCordis Corp.

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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