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FDA 510(k)

NCA-200

K-Number: K931608 · 1993-06-22

Decision Date1993-06-22
Product CodeKHH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NCA-200 is the device name listed in this FDA 510(k) record. The listed applicant is Ics Medical Corp.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K931608. The device is classified under product code KHH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NCA-200?

NCA-200 is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Ics Medical Corp.. The 510(k) number is K931608.

When did NCA-200 receive FDA 510(k) clearance?

NCA-200 received FDA 510(k) clearance on 1993-06-22, under 510(k) number K931608.

Who is the listed applicant for NCA-200?

The FDA 510(k) record lists Ics Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NCA-200?

The FDA product code for NCA-200 is KHH.

Other records listing Ics Medical Corp. 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 10 devices →

Related Devices (Code: KHH)

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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