FDA 510(k)

EZ 502

K-Number: K844163 · 1985-03-11

Decision Date1985-03-11

Product CodeKIJ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

EZ 502 is the device name listed in this FDA 510(k) record. The listed applicant is Aeg Power Tool Corp.. It received FDA 510(k) clearance on 1985-03-11 under 510(k) number K844163. The device is classified under product code KIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ 502?

EZ 502 is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Aeg Power Tool Corp.. The 510(k) number is K844163.

When did EZ 502 receive FDA 510(k) clearance?

EZ 502 received FDA 510(k) clearance on 1985-03-11, under 510(k) number K844163.

Who is the listed applicant for EZ 502?

The FDA 510(k) record lists Aeg Power Tool Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ 502?

The FDA product code for EZ 502 is KIJ.

Other records listing Aeg Power Tool Corp. 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.

K844162EZ 505

Related Devices (Code: KIJ)

K163308SMARTOJeil Medical Corporation K112599INSURGICAL SINGLE USE POWER EQUIPMENTInsurgical, LLC K101563SMARTOJeil Medical Corporation K972367STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENTStryker Instruments K970378STRYKER 2115 REPLACEMENT BATTERY (2115)Implant Resource, Inc.K960711ACUMED BONE GRAFT SYSTEMAcu Med, Inc.

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.