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FDA 510(k)

ENHANCE SUPPORT HOSE

K-Number: K873280 · 1987-10-09

ApplicantKimberly-Clark Corp.
Decision Date1987-10-09
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENHANCE SUPPORT HOSE is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873280. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENHANCE SUPPORT HOSE?

ENHANCE SUPPORT HOSE is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K873280.

When did ENHANCE SUPPORT HOSE receive FDA 510(k) clearance?

ENHANCE SUPPORT HOSE received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873280.

Who is the listed applicant for ENHANCE SUPPORT HOSE?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENHANCE SUPPORT HOSE?

The FDA product code for ENHANCE SUPPORT HOSE is DWL.

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Related Devices (Code: DWL)

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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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