Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NEITZ SLIT LAMP SL-H1

K-Number: K951340 · 1995-04-10

ApplicantNeitz Instruments Company, Ltd.
Decision Date1995-04-10
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NEITZ SLIT LAMP SL-H1 is the device name listed in this FDA 510(k) record. The listed applicant is Neitz Instruments Company, Ltd.. It received FDA 510(k) clearance on 1995-04-10 under 510(k) number K951340. 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 NEITZ SLIT LAMP SL-H1?

NEITZ SLIT LAMP SL-H1 is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Neitz Instruments Company, Ltd.. The 510(k) number is K951340.

When did NEITZ SLIT LAMP SL-H1 receive FDA 510(k) clearance?

NEITZ SLIT LAMP SL-H1 received FDA 510(k) clearance on 1995-04-10, under 510(k) number K951340.

Who is the listed applicant for NEITZ SLIT LAMP SL-H1?

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

What is the FDA product code for NEITZ SLIT LAMP SL-H1?

The FDA product code for NEITZ SLIT LAMP SL-H1 is HJO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Neitz Instruments Company, 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.

K972440CATARACTSCREENER CT - SK951341NEITZ SLIT LAMP SL-H2K951337FIBER HEAD LIGHT FH-300K950788OTOSCOPE A-34K951338INDIRECT OPHTHALMOSCOPE VIDEO SYSTEM IO0 A TVK950795STREAK RETINOSCOPE RX-RP

View all 24 devices →

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.

↑