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FDA 510(k)

RESPROCESSED SERFAS ENERGY PROBE

K-Number: K121855 · 2012-08-16

ApplicantStryker Sustainability Solutions
Decision Date2012-08-16
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RESPROCESSED SERFAS ENERGY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2012-08-16 under 510(k) number K121855. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPROCESSED SERFAS ENERGY PROBE?

RESPROCESSED SERFAS ENERGY PROBE is a medical device that received FDA 510(k) clearance on 2012-08-16. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K121855.

When did RESPROCESSED SERFAS ENERGY PROBE receive FDA 510(k) clearance?

RESPROCESSED SERFAS ENERGY PROBE received FDA 510(k) clearance on 2012-08-16, under 510(k) number K121855.

Who is the listed applicant for RESPROCESSED SERFAS ENERGY PROBE?

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

What is the FDA product code for RESPROCESSED SERFAS ENERGY PROBE?

The FDA product code for RESPROCESSED SERFAS ENERGY PROBE is NUJ.

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Related Devices (Code: NUJ)

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.

K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)Surgical Instrument Service and Savings, Inc.K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLCK182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren

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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