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FDA 510(k)

MISONIX IRRIGATION SYSTEM MOEDL BC20P

K-Number: K013417 · 2002-01-10

ApplicantMisonix, Inc.
Decision Date2002-01-10
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MISONIX IRRIGATION SYSTEM MOEDL BC20P is the device name listed in this FDA 510(k) record. The listed applicant is Misonix, Inc.. It received FDA 510(k) clearance on 2002-01-10 under 510(k) number K013417. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MISONIX IRRIGATION SYSTEM MOEDL BC20P?

MISONIX IRRIGATION SYSTEM MOEDL BC20P is a medical device that received FDA 510(k) clearance on 2002-01-10. The listed applicant is Misonix, Inc.. The 510(k) number is K013417.

When did MISONIX IRRIGATION SYSTEM MOEDL BC20P receive FDA 510(k) clearance?

MISONIX IRRIGATION SYSTEM MOEDL BC20P received FDA 510(k) clearance on 2002-01-10, under 510(k) number K013417.

Who is the listed applicant for MISONIX IRRIGATION SYSTEM MOEDL BC20P?

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

What is the FDA product code for MISONIX IRRIGATION SYSTEM MOEDL BC20P?

The FDA product code for MISONIX IRRIGATION SYSTEM MOEDL BC20P is GBX.

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Other records listing Misonix, Inc. as applicant

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Related Devices (Code: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, Inc.K973703JACKSON-PRATT HEMADUCT WOUND DRAIN, JACKSON-PRATT GOLD HEMADUCT WOUND DRAINAllegiance Healthcare Corp.

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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