Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CARE BAND ANTIBACTERIAL BANDAGES

K-Number: K983368 · 1999-02-17

ApplicantAso Corp.
Decision Date1999-02-17
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARE BAND ANTIBACTERIAL BANDAGES is the device name listed in this FDA 510(k) record. The listed applicant is Aso Corp.. It received FDA 510(k) clearance on 1999-02-17 under 510(k) number K983368. 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 CARE BAND ANTIBACTERIAL BANDAGES?

CARE BAND ANTIBACTERIAL BANDAGES is a medical device that received FDA 510(k) clearance on 1999-02-17. The listed applicant is Aso Corp.. The 510(k) number is K983368.

When did CARE BAND ANTIBACTERIAL BANDAGES receive FDA 510(k) clearance?

CARE BAND ANTIBACTERIAL BANDAGES received FDA 510(k) clearance on 1999-02-17, under 510(k) number K983368.

Who is the listed applicant for CARE BAND ANTIBACTERIAL BANDAGES?

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

What is the FDA product code for CARE BAND ANTIBACTERIAL BANDAGES?

The FDA product code for CARE BAND ANTIBACTERIAL BANDAGES 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 Aso 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.

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

View on FDA Database →

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

↑