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FDA 510(k)

QUICK CHANGE MONTGOMERY STRAP

K-Number: K893569 · 1989-09-25

ApplicantMed-Dex Intl.
Decision Date1989-09-25
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUICK CHANGE MONTGOMERY STRAP is the device name listed in this FDA 510(k) record. The listed applicant is Med-Dex Intl.. It received FDA 510(k) clearance on 1989-09-25 under 510(k) number K893569. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK CHANGE MONTGOMERY STRAP?

QUICK CHANGE MONTGOMERY STRAP is a medical device that received FDA 510(k) clearance on 1989-09-25. The listed applicant is Med-Dex Intl.. The 510(k) number is K893569.

When did QUICK CHANGE MONTGOMERY STRAP receive FDA 510(k) clearance?

QUICK CHANGE MONTGOMERY STRAP received FDA 510(k) clearance on 1989-09-25, under 510(k) number K893569.

Who is the listed applicant for QUICK CHANGE MONTGOMERY STRAP?

The FDA 510(k) record lists Med-Dex Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICK CHANGE MONTGOMERY STRAP?

The FDA product code for QUICK CHANGE MONTGOMERY STRAP is KGX.

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 Med-Dex Intl. 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.

K884630MULTI-PURPOSE HOLDERK881083GENERAL PURPOSE KITK881084UTILITY CLAMP

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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