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FDA 510(k)

DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY

K-Number: K941468 · 1994-05-12

ApplicantClinical Resources, Inc.
Decision Date1994-05-12
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Resources, Inc.. It received FDA 510(k) clearance on 1994-05-12 under 510(k) number K941468. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY?

DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Clinical Resources, Inc.. The 510(k) number is K941468.

When did DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY receive FDA 510(k) clearance?

DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY received FDA 510(k) clearance on 1994-05-12, under 510(k) number K941468.

Who is the listed applicant for DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY?

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

What is the FDA product code for DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY?

The FDA product code for DEBRIDEMENT TRAY, INCISION AND DRAINAGE TRAY is FRG.

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Other records listing Clinical Resources, Inc. 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.

K941470TRACHEOSTOMY CARE KITK944882IRRIGATION TRAYK944881SKIN SCRUB TRAYK945020FLUFF GAUZE SPONGEK945019FLUFF GAUXZE ROLLK945021FLUFF GAUZE SPONGE

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Related Devices (Code: FRG)

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.

K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* HEAVY-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* STANDARD-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* H300W Sterilization Wrap with ASSURE-DRY* TechnologyO&M Halyard, Inc.K252823Dukal Crepe Paper Sterilization WrapDukal, LLCK253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap; HALYARD* SEQUENTIAL Sterilization Wrap; HALYARD* SMART-FOLD* Sterilization WrapO&M Halyard, Inc.K251347Sterilization Pouch/RollSterivic Medical Co., Ltd.K251177Self-Seal Sterilization Pouch and RollGuangdong Maidi Medical Co., Ltd.K250306Chex-All Sterilization Pouches and TubesPropper Manufacturing Co., 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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