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FDA 510(k)

FLUORESCENCE ILLUMINATOR ACCESSORY

K-Number: K770652 · 1977-07-06

ApplicantBausch & Lomb, Inc.
Decision Date1977-07-06
Product CodeIBK
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

FLUORESCENCE ILLUMINATOR ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1977-07-06 under 510(k) number K770652. The device is classified under product code IBK. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUORESCENCE ILLUMINATOR ACCESSORY?

FLUORESCENCE ILLUMINATOR ACCESSORY is a medical device that received FDA 510(k) clearance on 1977-07-06. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K770652.

When did FLUORESCENCE ILLUMINATOR ACCESSORY receive FDA 510(k) clearance?

FLUORESCENCE ILLUMINATOR ACCESSORY received FDA 510(k) clearance on 1977-07-06, under 510(k) number K770652.

Who is the listed applicant for FLUORESCENCE ILLUMINATOR ACCESSORY?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUORESCENCE ILLUMINATOR ACCESSORY?

The FDA product code for FLUORESCENCE ILLUMINATOR ACCESSORY is IBK.

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Other records listing Bausch & Lomb, Inc. 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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

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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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