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FDA 510(k)

SERIES SY DISPOSABLE ELECTROSURGICAL PAD

K-Number: K082204 · 2008-08-13

ApplicantVentlab Corp.
Decision Date2008-08-13
Product CodeODR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SERIES SY DISPOSABLE ELECTROSURGICAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 2008-08-13 under 510(k) number K082204. The device is classified under product code ODR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES SY DISPOSABLE ELECTROSURGICAL PAD?

SERIES SY DISPOSABLE ELECTROSURGICAL PAD is a medical device that received FDA 510(k) clearance on 2008-08-13. The listed applicant is Ventlab Corp.. The 510(k) number is K082204.

When did SERIES SY DISPOSABLE ELECTROSURGICAL PAD receive FDA 510(k) clearance?

SERIES SY DISPOSABLE ELECTROSURGICAL PAD received FDA 510(k) clearance on 2008-08-13, under 510(k) number K082204.

Who is the listed applicant for SERIES SY DISPOSABLE ELECTROSURGICAL PAD?

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

What is the FDA product code for SERIES SY DISPOSABLE ELECTROSURGICAL PAD?

The FDA product code for SERIES SY DISPOSABLE ELECTROSURGICAL PAD is ODR.

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Related Devices (Code: ODR)

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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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