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FDA 510(k)

TALIA LASER SLIT

K-Number: K930518 · 1994-01-25

ApplicantTalia Technology , Ltd.
Decision Date1994-01-25
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TALIA LASER SLIT is the device name listed in this FDA 510(k) record. The listed applicant is Talia Technology , Ltd.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K930518. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALIA LASER SLIT?

TALIA LASER SLIT is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Talia Technology , Ltd.. The 510(k) number is K930518.

When did TALIA LASER SLIT receive FDA 510(k) clearance?

TALIA LASER SLIT received FDA 510(k) clearance on 1994-01-25, under 510(k) number K930518.

Who is the listed applicant for TALIA LASER SLIT?

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

What is the FDA product code for TALIA LASER SLIT?

The FDA product code for TALIA LASER SLIT is HJO.

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Other records listing Talia Technology , 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.

K061674RTA 5 & RTA MODEL E RETINAL THICKNESS ANALYZERK041290RTA MODEL D RETINAL THICKNESS ANALYZERK031312RTA MODEL D RETINAL THICKNESS ANALYZERK000731MODIFICATION TO RTA RETINAL THICKNESS ANALYZERK964137RTA RETINAL THICKNESS ANALYZER

Related Devices (Code: HJO)

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.

K262637SLIT LAMP SL-D4 (Type: LED)Topcon CorporationK253834VISUREF 600Carl Zeiss Vision GmbHK231760HP-OCT (HP-OCT)Cylite Pty. , Ltd.K222372Kowa SL-19Kowa Company , Ltd.K193188MiiS Horus Eye Anterior CameraMedimaging Integrated Solution, Inc (Miis)K182306Sunkingdom Slit LampChongqing Sunkingdom Medical Instrument Co., Ltd.

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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