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FDA 510(k)

NONE-GENERIC

K-Number: K940725 · 1995-04-18

Decision Date1995-04-18
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NONE-GENERIC is the device name listed in this FDA 510(k) record. The listed applicant is Yon'S Jay Enterprise Co.. It received FDA 510(k) clearance on 1995-04-18 under 510(k) number K940725. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NONE-GENERIC?

NONE-GENERIC is a medical device that received FDA 510(k) clearance on 1995-04-18. The listed applicant is Yon'S Jay Enterprise Co.. The 510(k) number is K940725.

When did NONE-GENERIC receive FDA 510(k) clearance?

NONE-GENERIC received FDA 510(k) clearance on 1995-04-18, under 510(k) number K940725.

Who is the listed applicant for NONE-GENERIC?

The FDA 510(k) record lists Yon'S Jay Enterprise Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONE-GENERIC?

The FDA product code for NONE-GENERIC is HQY.

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 Yon'S Jay Enterprise Co. 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: HQY)

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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