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FDA 510(k)

ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT

K-Number: K080202 · 2008-05-08

ApplicantOncobionics, Inc.
Decision Date2008-05-08
Product CodeOAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT is the device name listed in this FDA 510(k) record. The listed applicant is Oncobionics, Inc.. It received FDA 510(k) clearance on 2008-05-08 under 510(k) number K080202. The device is classified under product code OAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT?

ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT is a medical device that received FDA 510(k) clearance on 2008-05-08. The listed applicant is Oncobionics, Inc.. The 510(k) number is K080202.

When did ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT receive FDA 510(k) clearance?

ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT received FDA 510(k) clearance on 2008-05-08, under 510(k) number K080202.

Who is the listed applicant for ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT?

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

What is the FDA product code for ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT?

The FDA product code for ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT is OAB.

Related Clinical Trials

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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Other records listing Oncobionics, 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.

K060054ONCOBIONIC SYSTEM

Related Devices (Code: OAB)

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

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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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