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FDA 510(k)

NURTURE III

K-Number: K924312 · 1995-05-11

Decision Date1995-05-11
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NURTURE III is the device name listed in this FDA 510(k) record. The listed applicant is Bailey Medical Engineering. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K924312. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NURTURE III?

NURTURE III is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is Bailey Medical Engineering. The 510(k) number is K924312.

When did NURTURE III receive FDA 510(k) clearance?

NURTURE III received FDA 510(k) clearance on 1995-05-11, under 510(k) number K924312.

Who is the listed applicant for NURTURE III?

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

What is the FDA product code for NURTURE III?

The FDA product code for NURTURE III is HGX.

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 Bailey Medical Engineering 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: HGX)

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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