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FDA 510(k)

MR. RAZOR II TWIN

K-Number: K882388 · 1988-07-13

ApplicantBurney Products Corp.
Decision Date1988-07-13
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MR. RAZOR II TWIN is the device name listed in this FDA 510(k) record. The listed applicant is Burney Products Corp.. It received FDA 510(k) clearance on 1988-07-13 under 510(k) number K882388. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR. RAZOR II TWIN?

MR. RAZOR II TWIN is a medical device that received FDA 510(k) clearance on 1988-07-13. The listed applicant is Burney Products Corp.. The 510(k) number is K882388.

When did MR. RAZOR II TWIN receive FDA 510(k) clearance?

MR. RAZOR II TWIN received FDA 510(k) clearance on 1988-07-13, under 510(k) number K882388.

Who is the listed applicant for MR. RAZOR II TWIN?

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

What is the FDA product code for MR. RAZOR II TWIN?

The FDA product code for MR. RAZOR II TWIN is LDQ.

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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.

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