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FDA 510(k)

AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08

K-Number: K974467 · 1998-02-19

ApplicantAesculap-Meditec North America
Decision Date1998-02-19
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap-Meditec North America. It received FDA 510(k) clearance on 1998-02-19 under 510(k) number K974467. 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 AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08?

AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 is a medical device that received FDA 510(k) clearance on 1998-02-19. The listed applicant is Aesculap-Meditec North America. The 510(k) number is K974467.

When did AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 receive FDA 510(k) clearance?

AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 received FDA 510(k) clearance on 1998-02-19, under 510(k) number K974467.

Who is the listed applicant for AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08?

The FDA 510(k) record lists Aesculap-Meditec North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08?

The FDA product code for AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 is HJO.

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Other records listing Aesculap-Meditec North America as applicant

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K994116LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM)K992707MCL 29 DERMABLATE ER:YAG LASER SYSTEMK991285LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODEK981196MEDITEC LINKK980361DERMABLATE ER: YAG LASER SYSTEM

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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