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FDA 510(k)

MER MULTIPLANE RECTAL PROBE (MRP)

K-Number: K901033 · 1990-08-22

ApplicantMedical Equipment Resources
Decision Date1990-08-22
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MER MULTIPLANE RECTAL PROBE (MRP) 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 K901033. 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 MER MULTIPLANE RECTAL PROBE (MRP)?

MER MULTIPLANE RECTAL PROBE (MRP) 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 K901033.

When did MER MULTIPLANE RECTAL PROBE (MRP) receive FDA 510(k) clearance?

MER MULTIPLANE RECTAL PROBE (MRP) received FDA 510(k) clearance on 1990-08-22, under 510(k) number K901033.

Who is the listed applicant for MER MULTIPLANE RECTAL PROBE (MRP)?

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 RECTAL PROBE (MRP)?

The FDA product code for MER MULTIPLANE RECTAL PROBE (MRP) is IYO.

Related Clinical Trials

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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.

K901142MER MULTIPLANE VAGINAL PROBE (MVP)

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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