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FDA 510(k)

MER MULTIPLANE VAGINAL PROBE (MVP)

K-Number: K901142 · 1990-08-22

ApplicantMedical Equipment Resources
Decision Date1990-08-22
Product CodeHGL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MER MULTIPLANE VAGINAL PROBE (MVP) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Resources. It received FDA 510(k) clearance on 1990-08-22 under 510(k) number K901142. The device is classified under product code HGL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MER MULTIPLANE VAGINAL PROBE (MVP)?

MER MULTIPLANE VAGINAL PROBE (MVP) is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Medical Equipment Resources. The 510(k) number is K901142.

When did MER MULTIPLANE VAGINAL PROBE (MVP) receive FDA 510(k) clearance?

MER MULTIPLANE VAGINAL PROBE (MVP) received FDA 510(k) clearance on 1990-08-22, under 510(k) number K901142.

Who is the listed applicant for MER MULTIPLANE VAGINAL PROBE (MVP)?

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

What is the FDA product code for MER MULTIPLANE VAGINAL PROBE (MVP)?

The FDA product code for MER MULTIPLANE VAGINAL PROBE (MVP) is HGL.

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 Medical Equipment Resources 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.

K901033MER MULTIPLANE RECTAL PROBE (MRP)

Related Devices (Code: HGL)

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.

K952031ULTRASOUND TRANSDUCER, MODEL US917Advanced Medical Systems, Inc.K923335ULTRASOUND TRANSUCER, MODEL US915 -- MODIFICATIONAdvanced Medical Systems, Inc.K924516OP3/VP4Huntleigh Technology, Inc.K903348ULTRASONIC PULSED DOPPLER IMAGING SYSTEMAdvanced Technology Laboratories, Inc.K900966EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBEHitachi Medical Corp. of AmericaK903316ALOKA UST-964P-5 ENDOVAGINAL TRANSDUCERGe Medical Systems Information Technologies

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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