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FDA 510(k)

VALLEYLAB CURRENT MONITOR, E3350 & E3351

K-Number: K926415 · 1993-04-23

ApplicantValleylab, Inc.
Decision Date1993-04-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB CURRENT MONITOR, E3350 & E3351 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K926415. 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 VALLEYLAB CURRENT MONITOR, E3350 & E3351?

VALLEYLAB CURRENT MONITOR, E3350 & E3351 is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Valleylab, Inc.. The 510(k) number is K926415.

When did VALLEYLAB CURRENT MONITOR, E3350 & E3351 receive FDA 510(k) clearance?

VALLEYLAB CURRENT MONITOR, E3350 & E3351 received FDA 510(k) clearance on 1993-04-23, under 510(k) number K926415.

Who is the listed applicant for VALLEYLAB CURRENT MONITOR, E3350 & E3351?

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

What is the FDA product code for VALLEYLAB CURRENT MONITOR, E3350 & E3351?

The FDA product code for VALLEYLAB CURRENT MONITOR, E3350 & E3351 is GEI.

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Other records listing Valleylab, Inc. as applicant

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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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