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FDA 510(k)

MULTIPURPOSE TRANSDUCER RANGE

K-Number: K874192 · 1988-07-19

ApplicantPie Data Medical BV
Decision Date1988-07-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE TRANSDUCER RANGE is the device name listed in this FDA 510(k) record. The listed applicant is Pie Data Medical BV. It received FDA 510(k) clearance on 1988-07-19 under 510(k) number K874192. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPURPOSE TRANSDUCER RANGE?

MULTIPURPOSE TRANSDUCER RANGE is a medical device that received FDA 510(k) clearance on 1988-07-19. The listed applicant is Pie Data Medical BV. The 510(k) number is K874192.

When did MULTIPURPOSE TRANSDUCER RANGE receive FDA 510(k) clearance?

MULTIPURPOSE TRANSDUCER RANGE received FDA 510(k) clearance on 1988-07-19, under 510(k) number K874192.

Who is the listed applicant for MULTIPURPOSE TRANSDUCER RANGE?

The FDA 510(k) record lists Pie Data Medical BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPURPOSE TRANSDUCER RANGE?

The FDA product code for MULTIPURPOSE TRANSDUCER RANGE is IYO.

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 Pie Data Medical BV 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.

K870653ULTRASOUND LINEAR/SECTOR SCANNER 1100K870058PIE MEDICAL SCANNER 1000K874081ENTERSCANK871082FETAL CARE MONITOR ANTEPARTUM 1500

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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