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FDA 510(k)

B & L OPHTHALMIC INSTRUMENT STAND

K-Number: K791104 · 1979-07-24

ApplicantBausch & Lomb, Inc.
Decision Date1979-07-24
Product CodeHMF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

B & L OPHTHALMIC INSTRUMENT STAND 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 1979-07-24 under 510(k) number K791104. The device is classified under product code HMF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B & L OPHTHALMIC INSTRUMENT STAND?

B & L OPHTHALMIC INSTRUMENT STAND is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K791104.

When did B & L OPHTHALMIC INSTRUMENT STAND receive FDA 510(k) clearance?

B & L OPHTHALMIC INSTRUMENT STAND received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791104.

Who is the listed applicant for B & L OPHTHALMIC INSTRUMENT STAND?

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 B & L OPHTHALMIC INSTRUMENT STAND?

The FDA product code for B & L OPHTHALMIC INSTRUMENT STAND is HMF.

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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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Related Devices (Code: HMF)

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.

K935952ROTA SYSTEM 5000Rota Systems Medfurniture, Inc.K935945ROTA DATAMATE IRota Systems,Inc.K931839ROTA SYSTEM XLRota Systems Medfurniture, Inc.K930440MARCO INTERNATIONAL STANDMarco Ophthalmic, Inc.K924780BURTON OPHTHALMIC EXAM UNIT - MODEL 2201R.H. Burton Co.K924771BURTON OPHTHALMIC STAND - MODEL XL3200R.H. Burton Co.

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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