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FDA 510(k)

BURTON SLIT LAMP - MODEL 850

K-Number: K924783 · 1993-04-14

ApplicantR.H. Burton Co.
Decision Date1993-04-14
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BURTON SLIT LAMP - MODEL 850 is the device name listed in this FDA 510(k) record. The listed applicant is R.H. Burton Co.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K924783. 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 BURTON SLIT LAMP - MODEL 850?

BURTON SLIT LAMP - MODEL 850 is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is R.H. Burton Co.. The 510(k) number is K924783.

When did BURTON SLIT LAMP - MODEL 850 receive FDA 510(k) clearance?

BURTON SLIT LAMP - MODEL 850 received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924783.

Who is the listed applicant for BURTON SLIT LAMP - MODEL 850?

The FDA 510(k) record lists R.H. Burton Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURTON SLIT LAMP - MODEL 850?

The FDA product code for BURTON SLIT LAMP - MODEL 850 is HJO.

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Other records listing R.H. Burton Co. 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.

K924773BURTON H- BASE TABLE - MODEL 1990K924786BURTON TRIAL LENS SETK924774BURTON AUTOMATIC PROJECTOR - MODEL CP-40K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000K924784BURTON PROJECTOR HEAD - MODEL 6000-HK924778BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

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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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