FDA 510(k)

NT4-PLUS

K-Number: K932596 · 1993-08-12

Decision Date1993-08-12

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

NT4-PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Bmr Ent., Inc.. It received FDA 510(k) clearance on 1993-08-12 under 510(k) number K932596. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NT4-PLUS?

NT4-PLUS is a medical device that received FDA 510(k) clearance on 1993-08-12. The listed applicant is Bmr Ent., Inc.. The 510(k) number is K932596.

When did NT4-PLUS receive FDA 510(k) clearance?

NT4-PLUS received FDA 510(k) clearance on 1993-08-12, under 510(k) number K932596.

Who is the listed applicant for NT4-PLUS?

The FDA 510(k) record lists Bmr Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NT4-PLUS?

The FDA product code for NT4-PLUS is IPF.

Other records listing Bmr Ent., 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.

K933176NEUROTECH 2000 (NT2000)

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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.