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FDA 510(k)

E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH

K-Number: K970140 · 1997-03-28

ApplicantValleylab, Inc.
Decision Date1997-03-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1997-03-28 under 510(k) number K970140. 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 E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH?

E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH is a medical device that received FDA 510(k) clearance on 1997-03-28. The listed applicant is Valleylab, Inc.. The 510(k) number is K970140.

When did E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH receive FDA 510(k) clearance?

E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH received FDA 510(k) clearance on 1997-03-28, under 510(k) number K970140.

Who is the listed applicant for E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH?

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 E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH?

The FDA product code for E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH is GEI.

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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