FDA 510(k)

EZ 505

K-Number: K844162 · 1985-03-11

Decision Date1985-03-11

Product CodeKIJ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

EZ 505 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 K844162. 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 505?

EZ 505 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 K844162.

When did EZ 505 receive FDA 510(k) clearance?

EZ 505 received FDA 510(k) clearance on 1985-03-11, under 510(k) number K844162.

Who is the listed applicant for EZ 505?

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 505?

The FDA product code for EZ 505 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.

K844163EZ 502

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.