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FDA 510(k)

CLEANBLADE

K-Number: K931480 · 1993-07-23

ApplicantCleanblade, Inc.
Decision Date1993-07-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEANBLADE is the device name listed in this FDA 510(k) record. The listed applicant is Cleanblade, Inc.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K931480. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANBLADE?

CLEANBLADE is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Cleanblade, Inc.. The 510(k) number is K931480.

When did CLEANBLADE receive FDA 510(k) clearance?

CLEANBLADE received FDA 510(k) clearance on 1993-07-23, under 510(k) number K931480.

Who is the listed applicant for CLEANBLADE?

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

What is the FDA product code for CLEANBLADE?

The FDA product code for CLEANBLADE is GEI.

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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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