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FDA 510(k)

AMX-110, AMX-II AND AMX-III

K-Number: K884340 · 1989-01-24

ApplicantDyna-Med
Decision Date1989-01-24
Product CodeILZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AMX-110, AMX-II AND AMX-III is the device name listed in this FDA 510(k) record. The listed applicant is Dyna-Med. It received FDA 510(k) clearance on 1989-01-24 under 510(k) number K884340. The device is classified under product code ILZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMX-110, AMX-II AND AMX-III?

AMX-110, AMX-II AND AMX-III is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Dyna-Med. The 510(k) number is K884340.

When did AMX-110, AMX-II AND AMX-III receive FDA 510(k) clearance?

AMX-110, AMX-II AND AMX-III received FDA 510(k) clearance on 1989-01-24, under 510(k) number K884340.

Who is the listed applicant for AMX-110, AMX-II AND AMX-III?

The FDA 510(k) record lists Dyna-Med as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMX-110, AMX-II AND AMX-III?

The FDA product code for AMX-110, AMX-II AND AMX-III is ILZ.

Other records listing Dyna-Med 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.

K884578POLARIX 2 AND POLARIX 2EK863504OBSTETRICAL KITK760258BITE STICK, DYNA

Related Devices (Code: ILZ)

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.

K921711FLEXION DISTRATION SUPPORTAltoona Medical SupplyK895382VIBRA-TRAC TRACTION TABLEVibra-Trac IndustriesK852398VECTOR BAR SUSPENSION/TRACTION UNITPowlan Manufacturing Co.K844490TRACTION ACCESSORIESJerome MedicalK831135SAUNDERS #7080 CERVICAL TRACTION SYSChattanooga Group, Inc.K830245HEAD HALTERWarm & Form, Orthopedic Materials

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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