MICRO-DISPENSER 7000 & MICRODISPENSER 8000
K-Number: K954722 · 1996-01-16
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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