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FDA 510(k)

KENDALL UNIVERSAL EXTENSION SET

K-Number: K930551 · 1993-05-12

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1993-05-12
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KENDALL UNIVERSAL EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K930551. 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 KENDALL UNIVERSAL EXTENSION SET?

KENDALL UNIVERSAL EXTENSION SET is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K930551.

When did KENDALL UNIVERSAL EXTENSION SET receive FDA 510(k) clearance?

KENDALL UNIVERSAL EXTENSION SET received FDA 510(k) clearance on 1993-05-12, under 510(k) number K930551.

Who is the listed applicant for KENDALL UNIVERSAL EXTENSION SET?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL UNIVERSAL EXTENSION SET?

The FDA product code for KENDALL UNIVERSAL EXTENSION SET is GBX.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health as applicant

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.

K973763KENDALL CURITY IODOFORM PACKING STRIPK973511KENDALL CURITY PETROLATUM GAUZEK973507KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)K973619KENDALL CURITY NON-ADHERING DRESSINGK973509KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSINGK973546KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER

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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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