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FDA 510(k)

ACCU-SOURCE

K-Number: K051753 · 2006-03-29

ApplicantOncology Systems, Inc.
Decision Date2006-03-29
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCU-SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Oncology Systems, Inc.. It received FDA 510(k) clearance on 2006-03-29 under 510(k) number K051753. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-SOURCE?

ACCU-SOURCE is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Oncology Systems, Inc.. The 510(k) number is K051753.

When did ACCU-SOURCE receive FDA 510(k) clearance?

ACCU-SOURCE received FDA 510(k) clearance on 2006-03-29, under 510(k) number K051753.

Who is the listed applicant for ACCU-SOURCE?

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

What is the FDA product code for ACCU-SOURCE?

The FDA product code for ACCU-SOURCE is JAQ.

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Other records listing Oncology Systems, 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.

K123357ONQ RTSK092522ACU007SK871810PLAN-32 SOFTWARE

Related Devices (Code: JAQ)

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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