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FDA 510(k)

SUTURE REMOVAL KIT

K-Number: K914932 · 1992-01-31

ApplicantWestmark Hospital Supplies
Decision Date1992-01-31
Product CodeFRG
Advisory CommitteeHO
DecisionUnknown

Device Summary

SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Westmark Hospital Supplies. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K914932. 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 SUTURE REMOVAL KIT?

SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Westmark Hospital Supplies. The 510(k) number is K914932.

When did SUTURE REMOVAL KIT receive FDA 510(k) clearance?

SUTURE REMOVAL KIT received FDA 510(k) clearance on 1992-01-31, under 510(k) number K914932.

Who is the listed applicant for SUTURE REMOVAL KIT?

The FDA 510(k) record lists Westmark Hospital Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE REMOVAL KIT?

The FDA product code for SUTURE REMOVAL KIT is FRG.

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Other records listing Westmark Hospital Supplies 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.

K914934HAND PACKK914928BASIC SET UP TRAYK914935HEART PACK IIK914933HEART PACK IIIK914927DRESSING CHANGE KITK914929LACERATION TRAY

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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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