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FDA 510(k)

BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT

K-Number: K993138 · 1999-10-20

Decision Date1999-10-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ballard Medical Products. It received FDA 510(k) clearance on 1999-10-20 under 510(k) number K993138. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT?

BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT is a medical device that received FDA 510(k) clearance on 1999-10-20. The listed applicant is Ballard Medical Products. The 510(k) number is K993138.

When did BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT receive FDA 510(k) clearance?

BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT received FDA 510(k) clearance on 1999-10-20, under 510(k) number K993138.

Who is the listed applicant for BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT?

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

What is the FDA product code for BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT?

The FDA product code for BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT is KNT.

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 Ballard Medical Products 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.

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Related Devices (Code: KNT)

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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