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FDA 510(k)

260SL IMAGING SYSTEM SMALL PARTS PROBES

K-Number: K864136 · 1987-01-27

ApplicantGe Medical Systems Information Technologies
Decision Date1987-01-27
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

260SL IMAGING SYSTEM SMALL PARTS PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1987-01-27 under 510(k) number K864136. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 260SL IMAGING SYSTEM SMALL PARTS PROBES?

260SL IMAGING SYSTEM SMALL PARTS PROBES is a medical device that received FDA 510(k) clearance on 1987-01-27. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K864136.

When did 260SL IMAGING SYSTEM SMALL PARTS PROBES receive FDA 510(k) clearance?

260SL IMAGING SYSTEM SMALL PARTS PROBES received FDA 510(k) clearance on 1987-01-27, under 510(k) number K864136.

Who is the listed applicant for 260SL IMAGING SYSTEM SMALL PARTS PROBES?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 260SL IMAGING SYSTEM SMALL PARTS PROBES?

The FDA product code for 260SL IMAGING SYSTEM SMALL PARTS PROBES is ITX.

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Other records listing Ge Medical Systems Information Technologies 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.

K120770QT GUARD PLUS ANALYSIS SYSTEMK102426CARESCAPE MODEL V100 VITAL SIGNS MONITORK09236912SL ECG ANALYSIS PROGRAMK093141MARS HOLTER ANALYSIS WORKSTATIONK092027CARESCAPE MONITOR B850K090702MODIFICATION TO DASH 2500 PATIENT MONITOR

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Related Devices (Code: ITX)

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K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, Inc.

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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