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FDA 510(k)

SATURN 3 LASER SYSTEM

K-Number: K060764 · 2007-03-12

ApplicantResearch Instruments , Ltd.
Decision Date2007-03-12
Product CodeMRX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SATURN 3 LASER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Research Instruments , Ltd.. It received FDA 510(k) clearance on 2007-03-12 under 510(k) number K060764. The device is classified under product code MRX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SATURN 3 LASER SYSTEM?

SATURN 3 LASER SYSTEM is a medical device that received FDA 510(k) clearance on 2007-03-12. The listed applicant is Research Instruments , Ltd.. The 510(k) number is K060764.

When did SATURN 3 LASER SYSTEM receive FDA 510(k) clearance?

SATURN 3 LASER SYSTEM received FDA 510(k) clearance on 2007-03-12, under 510(k) number K060764.

Who is the listed applicant for SATURN 3 LASER SYSTEM?

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

What is the FDA product code for SATURN 3 LASER SYSTEM?

The FDA product code for SATURN 3 LASER SYSTEM is MRX.

Related Clinical Trials

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Other records listing Research Instruments , Ltd. 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.

K112413RI MSC (MIGRATION SEDIMENTATION CHAMBER)K083208SATURN ACTIVE LASER SYSTEMK003142MICROMANIPULATORK991261ICSI INJECTION MICROPIPETTE (SPIKED & NON-SPIKED), ICSI HOLDING MICEOPIPETTE, ASSISTED HATCHING/ZONA DRILLING MICROPIPET

Related Devices (Code: MRX)

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.

K253333Assisted Reproduction Laser System (Model ILS-400M)Hua Yue Medical Technology Co., Ltd.K202241LYKOS Assisted Reproduction Laser with Dynamic Targeting System (DTS)Hamilton Thorne, Inc.K192008LaserShot M, NaviLaseVitrolife GmbHK120055HANILTON THORNE INFRARED LASER OPTICAL SYSTEM-ZILOS-TK HAMILTON THORNE INFRARED LASER OPTICAL SYSTEM-LYKOSHamilton Thorne, Inc.K083208SATURN ACTIVE LASER SYSTEMResearch Instruments , Ltd.K063636ZILOS-TKHamilton Thorne Biosciences

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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