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FDA 510(k)

NG SECURE

K-Number: K953375 · 1995-09-08

ApplicantM.C. Johnson Co., Inc.
Decision Date1995-09-08
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NG SECURE is the device name listed in this FDA 510(k) record. The listed applicant is M.C. Johnson Co., Inc.. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K953375. 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 NG SECURE?

NG SECURE is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is M.C. Johnson Co., Inc.. The 510(k) number is K953375.

When did NG SECURE receive FDA 510(k) clearance?

NG SECURE received FDA 510(k) clearance on 1995-09-08, under 510(k) number K953375.

Who is the listed applicant for NG SECURE?

The FDA 510(k) record lists M.C. Johnson Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NG SECURE?

The FDA product code for NG SECURE is KNT.

Related Clinical Trials

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Other records listing M.C. Johnson Co., Inc. 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.

K872525A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECHK832702POCKET AID

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.

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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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