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FDA 510(k)

DESERET POSITIONAL SUTURE WING

K-Number: K915495 · 1992-04-06

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-04-06
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET POSITIONAL SUTURE WING is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1992-04-06 under 510(k) number K915495. 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 DESERET POSITIONAL SUTURE WING?

DESERET POSITIONAL SUTURE WING is a medical device that received FDA 510(k) clearance on 1992-04-06. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K915495.

When did DESERET POSITIONAL SUTURE WING receive FDA 510(k) clearance?

DESERET POSITIONAL SUTURE WING received FDA 510(k) clearance on 1992-04-06, under 510(k) number K915495.

Who is the listed applicant for DESERET POSITIONAL SUTURE WING?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET POSITIONAL SUTURE WING?

The FDA product code for DESERET POSITIONAL SUTURE WING is KMK.

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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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