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FDA 510(k)

CARAPACE DEBRIDEMENT KITS

K-Number: K931669 · 1994-02-07

ApplicantCarapace, Inc.
Decision Date1994-02-07
Product CodeFRG
Advisory CommitteeHO
DecisionUnknown

Device Summary

CARAPACE DEBRIDEMENT KITS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K931669. 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 CARAPACE DEBRIDEMENT KITS?

CARAPACE DEBRIDEMENT KITS is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Carapace, Inc.. The 510(k) number is K931669.

When did CARAPACE DEBRIDEMENT KITS receive FDA 510(k) clearance?

CARAPACE DEBRIDEMENT KITS received FDA 510(k) clearance on 1994-02-07, under 510(k) number K931669.

Who is the listed applicant for CARAPACE DEBRIDEMENT KITS?

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

What is the FDA product code for CARAPACE DEBRIDEMENT KITS?

The FDA product code for CARAPACE DEBRIDEMENT KITS 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 Carapace, 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.

K931722CARAPACE LABOR AND DELIVERY SETSK931822CARAPACE PELVIC EXAM TRAYSK931729I.V. START KITK931820CARAPACE STILLWATER BOWL SETK931760CARAPACE PACKING GAUZE TRAYSK932653SWISSTEK 2000(TM) CAST REMOVAL SYSTEM

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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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