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FDA 510(k)

OCD2001

K-Number: K992935 · 2000-06-20

Decision Date2000-06-20
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OCD2001 is the device name listed in this FDA 510(k) record. The listed applicant is Contemporary Products, Inc.. It received FDA 510(k) clearance on 2000-06-20 under 510(k) number K992935. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCD2001?

OCD2001 is a medical device that received FDA 510(k) clearance on 2000-06-20. The listed applicant is Contemporary Products, Inc.. The 510(k) number is K992935.

When did OCD2001 receive FDA 510(k) clearance?

OCD2001 received FDA 510(k) clearance on 2000-06-20, under 510(k) number K992935.

Who is the listed applicant for OCD2001?

The FDA 510(k) record lists Contemporary Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OCD2001?

The FDA product code for OCD2001 is NFB.

Other records listing Contemporary Products, 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: NFB)

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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