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FDA 510(k)

CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT

K-Number: K962033 · 1996-09-27

Decision Date1996-09-27
Product CodeCEW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT is the device name listed in this FDA 510(k) record. The listed applicant is Nichols Institute Diagnostics. It received FDA 510(k) clearance on 1996-09-27 under 510(k) number K962033. The device is classified under product code CEW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT?

CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT is a medical device that received FDA 510(k) clearance on 1996-09-27. The listed applicant is Nichols Institute Diagnostics. The 510(k) number is K962033.

When did CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT receive FDA 510(k) clearance?

CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT received FDA 510(k) clearance on 1996-09-27, under 510(k) number K962033.

Who is the listed applicant for CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT?

The FDA 510(k) record lists Nichols Institute Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT?

The FDA product code for CHEMILUMINESCENCE INTRA-OPERATIVE INTACT PTH KIT is CEW.

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 Nichols Institute Diagnostics 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.

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Related Devices (Code: CEW)

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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