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FDA 510(k)

SHIPPERT PRESSURE BANDAGE

K-Number: K940798 · 1994-09-28

ApplicantDenver Splint Co.
Decision Date1994-09-28
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHIPPERT PRESSURE BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Denver Splint Co.. It received FDA 510(k) clearance on 1994-09-28 under 510(k) number K940798. 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 SHIPPERT PRESSURE BANDAGE?

SHIPPERT PRESSURE BANDAGE is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is Denver Splint Co.. The 510(k) number is K940798.

When did SHIPPERT PRESSURE BANDAGE receive FDA 510(k) clearance?

SHIPPERT PRESSURE BANDAGE received FDA 510(k) clearance on 1994-09-28, under 510(k) number K940798.

Who is the listed applicant for SHIPPERT PRESSURE BANDAGE?

The FDA 510(k) record lists Denver Splint Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHIPPERT PRESSURE BANDAGE?

The FDA product code for SHIPPERT PRESSURE BANDAGE 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 Denver Splint Co. 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.

K940133THE EXPANDACELL EAR PACKK935724THE EXPANDACELL SINUS PACKK922062THE DENVER CAUTERY

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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