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FDA 510(k)

MOTO-MED RF-II AND PICO

K-Number: K893924 · 1990-11-27

ApplicantHoll Meditronics, Inc.
Decision Date1990-11-27
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOTO-MED RF-II AND PICO is the device name listed in this FDA 510(k) record. The listed applicant is Holl Meditronics, Inc.. It received FDA 510(k) clearance on 1990-11-27 under 510(k) number K893924. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTO-MED RF-II AND PICO?

MOTO-MED RF-II AND PICO is a medical device that received FDA 510(k) clearance on 1990-11-27. The listed applicant is Holl Meditronics, Inc.. The 510(k) number is K893924.

When did MOTO-MED RF-II AND PICO receive FDA 510(k) clearance?

MOTO-MED RF-II AND PICO received FDA 510(k) clearance on 1990-11-27, under 510(k) number K893924.

Who is the listed applicant for MOTO-MED RF-II AND PICO?

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

What is the FDA product code for MOTO-MED RF-II AND PICO?

The FDA product code for MOTO-MED RF-II AND PICO is BXB.

Other records listing Holl Meditronics, 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.

K954171ARCO-MBC, ARCO MCK942095SONOCA IIIK911600ILCO INFRARED LIGHT COAGULATORK901737SONOCA II ULTRASONIC SURGICAL DEVICEK893926SONOCA ULTRASONIC SURGICAL SYSTEM

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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