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FDA 510(k)

LIBERATOR

K-Number: K925387 · 1993-03-29

ApplicantPrentke Romich Co.
Decision Date1993-03-29
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIBERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Prentke Romich Co.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K925387. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERATOR?

LIBERATOR is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Prentke Romich Co.. The 510(k) number is K925387.

When did LIBERATOR receive FDA 510(k) clearance?

LIBERATOR received FDA 510(k) clearance on 1993-03-29, under 510(k) number K925387.

Who is the listed applicant for LIBERATOR?

The FDA 510(k) record lists Prentke Romich Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIBERATOR?

The FDA product code for LIBERATOR is ILQ.

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Other records listing Prentke Romich Co. as applicant

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Related Devices (Code: ILQ)

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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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