NYNEX II
K-Number: K830932 · 1983-04-18
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Device Summary
Frequently Asked Questions
What is the NYNEX II?
NYNEX II is a medical device that received FDA 510(k) clearance on 1983-04-18. The listed applicant is La Jolla Technology, Inc.. The 510(k) number is K830932.
When did NYNEX II receive FDA 510(k) clearance?
NYNEX II received FDA 510(k) clearance on 1983-04-18, under 510(k) number K830932.
Who is the listed applicant for NYNEX II?
The FDA 510(k) record lists La Jolla Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NYNEX II?
The FDA product code for NYNEX II is GZJ.
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 La Jolla Technology, 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: GZJ)
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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