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FDA 510(k)

EZ MOVER

K-Number: K930324 · 1993-06-11

ApplicantPrime Ideas, Inc.
Decision Date1993-06-11
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EZ MOVER is the device name listed in this FDA 510(k) record. The listed applicant is Prime Ideas, Inc.. It received FDA 510(k) clearance on 1993-06-11 under 510(k) number K930324. 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 EZ MOVER?

EZ MOVER is a medical device that received FDA 510(k) clearance on 1993-06-11. The listed applicant is Prime Ideas, Inc.. The 510(k) number is K930324.

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

EZ MOVER received FDA 510(k) clearance on 1993-06-11, under 510(k) number K930324.

Who is the listed applicant for EZ MOVER?

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

What is the FDA product code for EZ MOVER?

The FDA product code for EZ MOVER is IYO.

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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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