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FDA 510(k)

HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE

K-Number: K922739 · 1992-08-06

ApplicantHollister, Inc.
Decision Date1992-08-06
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K922739. 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 HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE?

HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Hollister, Inc.. The 510(k) number is K922739.

When did HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE receive FDA 510(k) clearance?

HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE received FDA 510(k) clearance on 1992-08-06, under 510(k) number K922739.

Who is the listed applicant for HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE?

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

What is the FDA product code for HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE?

The FDA product code for HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE is GBX.

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Other records listing Hollister, 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.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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