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FDA 510(k)

PATLOG 2.0

K-Number: K092939 · 2009-10-09

ApplicantOncolog Medical QA AB
Decision Date2009-10-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PATLOG 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Oncolog Medical QA AB. It received FDA 510(k) clearance on 2009-10-09 under 510(k) number K092939. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATLOG 2.0?

PATLOG 2.0 is a medical device that received FDA 510(k) clearance on 2009-10-09. The listed applicant is Oncolog Medical QA AB. The 510(k) number is K092939.

When did PATLOG 2.0 receive FDA 510(k) clearance?

PATLOG 2.0 received FDA 510(k) clearance on 2009-10-09, under 510(k) number K092939.

Who is the listed applicant for PATLOG 2.0?

The FDA 510(k) record lists Oncolog Medical QA AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATLOG 2.0?

The FDA product code for PATLOG 2.0 is IYE.

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 Oncolog Medical QA AB 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.

K090044PATLOG, PATLOG PATIENT HANDLING SYSTEM, PATLOG TOPLOG TABLE TOP, MODEL(S) 1.0, 1.0, C

Related Devices (Code: IYE)

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.

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

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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