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FDA 510(k)

METRICON #120 FLUOROPHOTOMETER

K-Number: K802355 · 1980-12-17

ApplicantMetricon, Ltd.
Decision Date1980-12-17
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

METRICON #120 FLUOROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Metricon, Ltd.. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802355. 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 METRICON #120 FLUOROPHOTOMETER?

METRICON #120 FLUOROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Metricon, Ltd.. The 510(k) number is K802355.

When did METRICON #120 FLUOROPHOTOMETER receive FDA 510(k) clearance?

METRICON #120 FLUOROPHOTOMETER received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802355.

Who is the listed applicant for METRICON #120 FLUOROPHOTOMETER?

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

What is the FDA product code for METRICON #120 FLUOROPHOTOMETER?

The FDA product code for METRICON #120 FLUOROPHOTOMETER is HJO.

Related Clinical Trials

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Other records listing Metricon, 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.

K810562CARBON DIOXIDE (C02) MICROSURGICAL LASERK802034CO2 MICROSURGICAL LASER SYSTEM #370

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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