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FDA 510(k)

JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS

K-Number: K905614 · 1991-03-20

ApplicantBaxter Healthcare Corp
Decision Date1991-03-20
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1991-03-20 under 510(k) number K905614. 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 JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS?

JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS is a medical device that received FDA 510(k) clearance on 1991-03-20. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K905614.

When did JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS receive FDA 510(k) clearance?

JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS received FDA 510(k) clearance on 1991-03-20, under 510(k) number K905614.

Who is the listed applicant for JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS?

The FDA product code for JACKSON-PRATT, HIGH LUBRICITY AND WOUND DRAINS 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, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, Inc.

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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