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FDA 510(k)

AMSINO SUTURE REMOVAL KIT

K-Number: K050656 · 2005-05-02

ApplicantAmsino International, Inc.
Decision Date2005-05-02
Product CodeMCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMSINO SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Amsino International, Inc.. It received FDA 510(k) clearance on 2005-05-02 under 510(k) number K050656. The device is classified under product code MCZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSINO SUTURE REMOVAL KIT?

AMSINO SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 2005-05-02. The listed applicant is Amsino International, Inc.. The 510(k) number is K050656.

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

AMSINO SUTURE REMOVAL KIT received FDA 510(k) clearance on 2005-05-02, under 510(k) number K050656.

Who is the listed applicant for AMSINO SUTURE REMOVAL KIT?

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

What is the FDA product code for AMSINO SUTURE REMOVAL KIT?

The FDA product code for AMSINO SUTURE REMOVAL KIT is MCZ.

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Other records listing Amsino International, 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.

K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)K220230AMSure Enteral Feeding PumpK220267AMSafe NeuFlo Needleless ConnectorK213522AMSafe Pre-Filled Normal Saline Flush SyringeK200051PUGGLE Enteral Feeding Pump and Feeding SetK183473AMSafe(R) Pre-Filled Normal Saline Flush Syringe

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Related Devices (Code: MCZ)

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.

K964827PROD. NO. 01-132 - SUTURE REMOVAL KITContinental Medical Laboratories, Inc.K963714GRAND MEDICAL SUTURE REMOVAL KITGrand Medical ProductsK943046SKIN STAPLE REMOVAL TRAYSSterile Concepts, Inc.K941465SUTURE REMOVAL KITClinical Resources, Inc.K931597CARAPACE INCISION AND DRAINAGE TRAYSCarapace, Inc.K925015STERILE SUTURE REMOVAL KITCustomed, 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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