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FDA 510(k)

SWITCHBLADE

K-Number: K030890 · 2003-04-04

ApplicantSnowden Pencer, Inc.
Decision Date2003-04-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SWITCHBLADE is the device name listed in this FDA 510(k) record. The listed applicant is Snowden Pencer, Inc.. It received FDA 510(k) clearance on 2003-04-04 under 510(k) number K030890. 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 SWITCHBLADE?

SWITCHBLADE is a medical device that received FDA 510(k) clearance on 2003-04-04. The listed applicant is Snowden Pencer, Inc.. The 510(k) number is K030890.

When did SWITCHBLADE receive FDA 510(k) clearance?

SWITCHBLADE received FDA 510(k) clearance on 2003-04-04, under 510(k) number K030890.

Who is the listed applicant for SWITCHBLADE?

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

What is the FDA product code for SWITCHBLADE?

The FDA product code for SWITCHBLADE is GEI.

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Related Devices (Code: 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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