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FDA 510(k)

CENTERMARK SECURING WINGS

K-Number: K940127 · 1994-02-09

ApplicantMenlo Care, Inc.
Decision Date1994-02-09
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTERMARK SECURING WINGS is the device name listed in this FDA 510(k) record. The listed applicant is Menlo Care, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K940127. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTERMARK SECURING WINGS?

CENTERMARK SECURING WINGS is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Menlo Care, Inc.. The 510(k) number is K940127.

When did CENTERMARK SECURING WINGS receive FDA 510(k) clearance?

CENTERMARK SECURING WINGS received FDA 510(k) clearance on 1994-02-09, under 510(k) number K940127.

Who is the listed applicant for CENTERMARK SECURING WINGS?

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

What is the FDA product code for CENTERMARK SECURING WINGS?

The FDA product code for CENTERMARK SECURING WINGS is KMK.

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Other records listing Menlo Care, 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.

K964447PICC CATHETER/MIDLINE CATHETERK951620MIDMARK MIDLINE CATHETERK945521CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAYK950737LANDMARK MIDLINE CATHETERK944968LANDMARK MIDLINE CATHETERK943893PERCUTANEOUS GRAINAGE CATHETER

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Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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