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FDA 510(k)

MICRO-DISPENSER 7000 & MICRODISPENSER 8000

K-Number: K954722 · 1996-01-16

ApplicantNOUVAG AG
Decision Date1996-01-16
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO-DISPENSER 7000 & MICRODISPENSER 8000 is the device name listed in this FDA 510(k) record. The listed applicant is NOUVAG AG. It received FDA 510(k) clearance on 1996-01-16 under 510(k) number K954722. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-DISPENSER 7000 & MICRODISPENSER 8000?

MICRO-DISPENSER 7000 & MICRODISPENSER 8000 is a medical device that received FDA 510(k) clearance on 1996-01-16. The listed applicant is NOUVAG AG. The 510(k) number is K954722.

When did MICRO-DISPENSER 7000 & MICRODISPENSER 8000 receive FDA 510(k) clearance?

MICRO-DISPENSER 7000 & MICRODISPENSER 8000 received FDA 510(k) clearance on 1996-01-16, under 510(k) number K954722.

Who is the listed applicant for MICRO-DISPENSER 7000 & MICRODISPENSER 8000?

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

What is the FDA product code for MICRO-DISPENSER 7000 & MICRODISPENSER 8000?

The FDA product code for MICRO-DISPENSER 7000 & MICRODISPENSER 8000 is EFB.

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 NOUVAG AG 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.

View all 12 devices →

Related Devices (Code: EFB)

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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