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FDA 510(k)

DISPOSABLE LATEX BANDAGE

K-Number: K842301 · 1984-11-05

ApplicantInmed Corp.
Decision Date1984-11-05
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE LATEX BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K842301. 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 DISPOSABLE LATEX BANDAGE?

DISPOSABLE LATEX BANDAGE is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Inmed Corp.. The 510(k) number is K842301.

When did DISPOSABLE LATEX BANDAGE receive FDA 510(k) clearance?

DISPOSABLE LATEX BANDAGE received FDA 510(k) clearance on 1984-11-05, under 510(k) number K842301.

Who is the listed applicant for DISPOSABLE LATEX BANDAGE?

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

What is the FDA product code for DISPOSABLE LATEX BANDAGE?

The FDA product code for DISPOSABLE LATEX 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.

Other records listing Inmed Corp. 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.

View all 32 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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