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FDA 510(k)

METAPAK MULTI-PURPOSE INSTRUMENT TRAY

K-Number: K993535 · 2001-12-07

ApplicantRiley Medical, Inc.
Decision Date2001-12-07
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

METAPAK MULTI-PURPOSE INSTRUMENT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Riley Medical, Inc.. It received FDA 510(k) clearance on 2001-12-07 under 510(k) number K993535. 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 METAPAK MULTI-PURPOSE INSTRUMENT TRAY?

METAPAK MULTI-PURPOSE INSTRUMENT TRAY is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Riley Medical, Inc.. The 510(k) number is K993535.

When did METAPAK MULTI-PURPOSE INSTRUMENT TRAY receive FDA 510(k) clearance?

METAPAK MULTI-PURPOSE INSTRUMENT TRAY received FDA 510(k) clearance on 2001-12-07, under 510(k) number K993535.

Who is the listed applicant for METAPAK MULTI-PURPOSE INSTRUMENT TRAY?

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

What is the FDA product code for METAPAK MULTI-PURPOSE INSTRUMENT TRAY?

The FDA product code for METAPAK MULTI-PURPOSE INSTRUMENT TRAY is FRG.

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Other records listing Riley Medical, 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.

K944025SURGICAL INSTRUMENT TRAY

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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