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FDA 510(k)

BC 900 SLIT LAMP

K-Number: K982057 · 1998-08-14

ApplicantHaag-Streit AG
Decision Date1998-08-14
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BC 900 SLIT LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Haag-Streit AG. It received FDA 510(k) clearance on 1998-08-14 under 510(k) number K982057. 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 BC 900 SLIT LAMP?

BC 900 SLIT LAMP is a medical device that received FDA 510(k) clearance on 1998-08-14. The listed applicant is Haag-Streit AG. The 510(k) number is K982057.

When did BC 900 SLIT LAMP receive FDA 510(k) clearance?

BC 900 SLIT LAMP received FDA 510(k) clearance on 1998-08-14, under 510(k) number K982057.

Who is the listed applicant for BC 900 SLIT LAMP?

The FDA 510(k) record lists Haag-Streit AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BC 900 SLIT LAMP?

The FDA product code for BC 900 SLIT LAMP is HJO.

Other records listing Haag-Streit AG 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.

K100202SLIT LAMP BO 900, BQ 900, BP900K082891LENSTAR, MODEL LS900

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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