NITRO
K-Number: K940304 · 1994-02-17
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Device Summary
Frequently Asked Questions
What is the NITRO?
NITRO is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K940304.
When did NITRO receive FDA 510(k) clearance?
NITRO received FDA 510(k) clearance on 1994-02-17, under 510(k) number K940304.
Who is the listed applicant for NITRO?
The FDA 510(k) record lists Everest & Jennings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NITRO?
The FDA product code for NITRO is IOR.
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 Everest & Jennings, 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.
Related Devices (Code: IOR)
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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