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FDA 510(k)

BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION

K-Number: K024289 · 2003-05-02

ApplicantBausch & Lomb, Incorporated
Decision Date2003-05-02
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Incorporated. It received FDA 510(k) clearance on 2003-05-02 under 510(k) number K024289. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION?

BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION is a medical device that received FDA 510(k) clearance on 2003-05-02. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K024289.

When did BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION receive FDA 510(k) clearance?

BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION received FDA 510(k) clearance on 2003-05-02, under 510(k) number K024289.

Who is the listed applicant for BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION?

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

What is the FDA product code for BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION?

The FDA product code for BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION is MRC.

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Related Devices (Code: MRC)

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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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