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FDA 510(k)

ELECTROCAUTERY PROBE

K-Number: K910334 · 1991-02-21

ApplicantWiltek Medical, Inc.
Decision Date1991-02-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROCAUTERY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Wiltek Medical, Inc.. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K910334. 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 ELECTROCAUTERY PROBE?

ELECTROCAUTERY PROBE is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Wiltek Medical, Inc.. The 510(k) number is K910334.

When did ELECTROCAUTERY PROBE receive FDA 510(k) clearance?

ELECTROCAUTERY PROBE received FDA 510(k) clearance on 1991-02-21, under 510(k) number K910334.

Who is the listed applicant for ELECTROCAUTERY PROBE?

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

What is the FDA product code for ELECTROCAUTERY PROBE?

The FDA product code for ELECTROCAUTERY PROBE is GEI.

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Other records listing Wiltek Medical, Inc. as applicant

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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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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