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FDA 510(k)

NIC OPTRONICS CS-2000

K-Number: K822215 · 1982-08-31

Decision Date1982-08-31
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NIC OPTRONICS CS-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical Instruments. It received FDA 510(k) clearance on 1982-08-31 under 510(k) number K822215. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIC OPTRONICS CS-2000?

NIC OPTRONICS CS-2000 is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is Nicolet Biomedical Instruments. The 510(k) number is K822215.

When did NIC OPTRONICS CS-2000 receive FDA 510(k) clearance?

NIC OPTRONICS CS-2000 received FDA 510(k) clearance on 1982-08-31, under 510(k) number K822215.

Who is the listed applicant for NIC OPTRONICS CS-2000?

The FDA 510(k) record lists Nicolet Biomedical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIC OPTRONICS CS-2000?

The FDA product code for NIC OPTRONICS CS-2000 is HOX.

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 Nicolet Biomedical Instruments 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 26 devices →

Related Devices (Code: HOX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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