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FDA 510(k)

MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50

K-Number: K980980 · 1998-06-15

ApplicantKonigsberg Instruments, Inc.
Decision Date1998-06-15
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 is the device name listed in this FDA 510(k) record. The listed applicant is Konigsberg Instruments, Inc.. It received FDA 510(k) clearance on 1998-06-15 under 510(k) number K980980. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50?

MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 is a medical device that received FDA 510(k) clearance on 1998-06-15. The listed applicant is Konigsberg Instruments, Inc.. The 510(k) number is K980980.

When did MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 receive FDA 510(k) clearance?

MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 received FDA 510(k) clearance on 1998-06-15, under 510(k) number K980980.

Who is the listed applicant for MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50?

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

What is the FDA product code for MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50?

The FDA product code for MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 is FFX.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Konigsberg 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.

K813331P51 ANGIOPLASTY PRESSURE TRANSDUCERK811083ESOPHAGEAL MOTILITY PROBE

Related Devices (Code: FFX)

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.

K252605mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001)Medspira, LLCK240007Solar Compact (G4-1)Laborie Medical Technologies, Corp.K231861EndoflipTM 300 SystemCovidien, LLCK223705EndoflipTM 300Covidien, LLCK222000Transit-PelletsMedifactia ABK201106IntraMarX 3D Radiopaque MarkerAnx Robotica Corp

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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