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FDA 510(k)

MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM

K-Number: K131247 · 2013-08-14

ApplicantMfs - Medical Flow Systems, Ltd.
Decision Date2013-08-14
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mfs - Medical Flow Systems, Ltd.. It received FDA 510(k) clearance on 2013-08-14 under 510(k) number K131247. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM?

MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2013-08-14. The listed applicant is Mfs - Medical Flow Systems, Ltd.. The 510(k) number is K131247.

When did MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM receive FDA 510(k) clearance?

MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM received FDA 510(k) clearance on 2013-08-14, under 510(k) number K131247.

Who is the listed applicant for MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM?

The FDA 510(k) record lists Mfs - Medical Flow Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM?

The FDA product code for MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM is MEB.

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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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