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FDA 510(k)

VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM

K-Number: K002402 · 2000-08-31

ApplicantMitek Products
Decision Date2000-08-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Products. It received FDA 510(k) clearance on 2000-08-31 under 510(k) number K002402. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM?

VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 2000-08-31. The listed applicant is Mitek Products. The 510(k) number is K002402.

When did VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM receive FDA 510(k) clearance?

VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM received FDA 510(k) clearance on 2000-08-31, under 510(k) number K002402.

Who is the listed applicant for VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM?

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

What is the FDA product code for VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM?

The FDA product code for VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM is HRX.

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Other records listing Mitek Products as applicant

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Related Devices (Code: HRX)

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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