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FDA 510(k)

NITRO

K-Number: K940304 · 1994-02-17

Decision Date1994-02-17
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NITRO is the device name listed in this FDA 510(k) record. The listed applicant is Everest & Jennings, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K940304. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 30 devices →

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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