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FDA 510(k)

REMUSK MP

K-Number: K922029 · 1992-10-06

ApplicantEquipement Biomedical Specialise, Inc.
Decision Date1992-10-06
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REMUSK MP is the device name listed in this FDA 510(k) record. The listed applicant is Equipement Biomedical Specialise, Inc.. It received FDA 510(k) clearance on 1992-10-06 under 510(k) number K922029. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMUSK MP?

REMUSK MP is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Equipement Biomedical Specialise, Inc.. The 510(k) number is K922029.

When did REMUSK MP receive FDA 510(k) clearance?

REMUSK MP received FDA 510(k) clearance on 1992-10-06, under 510(k) number K922029.

Who is the listed applicant for REMUSK MP?

The FDA 510(k) record lists Equipement Biomedical Specialise, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REMUSK MP?

The FDA product code for REMUSK MP is LBB.

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Related Devices (Code: LBB)

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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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