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FDA 510(k)

VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)

K-Number: K993039 · 2000-01-07

ApplicantBausch & Lomb, Inc.
Decision Date2000-01-07
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700) 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 2000-01-07 under 510(k) number K993039. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)?

VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700) is a medical device that received FDA 510(k) clearance on 2000-01-07. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K993039.

When did VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700) receive FDA 510(k) clearance?

VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700) received FDA 510(k) clearance on 2000-01-07, under 510(k) number K993039.

Who is the listed applicant for VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)?

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 VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)?

The FDA product code for VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700) is MRH.

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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.

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Related Devices (Code: MRH)

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.

K253760OMNI Ultra Surgical System (1-110)Sight Sciences, Inc.K243503VIA360™ Surgical SystemNew World Medical, Inc.K232214OMNI Surgical SystemSight Sciences, Inc.K213173TrabEx ProMicrosurgical Technologies, Inc.K212797iPrime Viscodelivery SystemGlaukosK211680Streamline Surgical SystemNew World Medical, Inc.

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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