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FDA 510(k)

OR PREP KIT

K-Number: K830476 · 1983-03-31

ApplicantClinipad Corp.
Decision Date1983-03-31
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OR PREP KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clinipad Corp.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830476. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OR PREP KIT?

OR PREP KIT is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Clinipad Corp.. The 510(k) number is K830476.

When did OR PREP KIT receive FDA 510(k) clearance?

OR PREP KIT received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830476.

Who is the listed applicant for OR PREP KIT?

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

What is the FDA product code for OR PREP KIT?

The FDA product code for OR PREP KIT is FRG.

Other records listing Clinipad Corp. as applicant

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Related Devices (Code: FRG)

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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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