Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NYNEX II

K-Number: K830932 · 1983-04-18

Decision Date1983-04-18
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NYNEX II is the device name listed in this FDA 510(k) record. The listed applicant is La Jolla Technology, Inc.. It received FDA 510(k) clearance on 1983-04-18 under 510(k) number K830932. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

↑