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FDA 510(k)

DEUTSCH ANTI-BLOCKAGE WOUND DRAIN

K-Number: K052286 · 2005-10-21

ApplicantThe Catheter Exchange, Inc.
Decision Date2005-10-21
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEUTSCH ANTI-BLOCKAGE WOUND DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is The Catheter Exchange, Inc.. It received FDA 510(k) clearance on 2005-10-21 under 510(k) number K052286. 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 DEUTSCH ANTI-BLOCKAGE WOUND DRAIN?

DEUTSCH ANTI-BLOCKAGE WOUND DRAIN is a medical device that received FDA 510(k) clearance on 2005-10-21. The listed applicant is The Catheter Exchange, Inc.. The 510(k) number is K052286.

When did DEUTSCH ANTI-BLOCKAGE WOUND DRAIN receive FDA 510(k) clearance?

DEUTSCH ANTI-BLOCKAGE WOUND DRAIN received FDA 510(k) clearance on 2005-10-21, under 510(k) number K052286.

Who is the listed applicant for DEUTSCH ANTI-BLOCKAGE WOUND DRAIN?

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

What is the FDA product code for DEUTSCH ANTI-BLOCKAGE WOUND DRAIN?

The FDA product code for DEUTSCH ANTI-BLOCKAGE WOUND DRAIN is GBX.

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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, LLCK043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, 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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