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FDA 510(k)

STERILE CENTRAL LINE DRESSING TRAY

K-Number: K934031 · 1994-03-01

ApplicantSurgipro, Inc.
Decision Date1994-03-01
Product CodeFRG
Advisory CommitteeHO
DecisionUnknown

Device Summary

STERILE CENTRAL LINE DRESSING TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Surgipro, Inc.. It received FDA 510(k) clearance on 1994-03-01 under 510(k) number K934031. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the STERILE CENTRAL LINE DRESSING TRAY?

STERILE CENTRAL LINE DRESSING TRAY is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Surgipro, Inc.. The 510(k) number is K934031.

When did STERILE CENTRAL LINE DRESSING TRAY receive FDA 510(k) clearance?

STERILE CENTRAL LINE DRESSING TRAY received FDA 510(k) clearance on 1994-03-01, under 510(k) number K934031.

Who is the listed applicant for STERILE CENTRAL LINE DRESSING TRAY?

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

What is the FDA product code for STERILE CENTRAL LINE DRESSING TRAY?

The FDA product code for STERILE CENTRAL LINE DRESSING TRAY is FRG.

Related Clinical Trials

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.

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Other records listing Surgipro, 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.

K934028STERILE DRESSING CHANGE TRAYK934029STERILE LACERATION & DEBRIDEMENT TRAYSK934030STERILE TRACHEOSTOMY TRAYK912351VARIOUS STERILE CUSTOM DRESSING TRAYS & KITS

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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