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FDA 510(k)

OROSCOPE MODEL NUMBER COS-100

K-Number: K903718 · 1990-11-09

Decision Date1990-11-09
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OROSCOPE MODEL NUMBER COS-100 is the device name listed in this FDA 510(k) record. The listed applicant is Cygnus Instruments, Inc.. It received FDA 510(k) clearance on 1990-11-09 under 510(k) number K903718. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OROSCOPE MODEL NUMBER COS-100?

OROSCOPE MODEL NUMBER COS-100 is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Cygnus Instruments, Inc.. The 510(k) number is K903718.

When did OROSCOPE MODEL NUMBER COS-100 receive FDA 510(k) clearance?

OROSCOPE MODEL NUMBER COS-100 received FDA 510(k) clearance on 1990-11-09, under 510(k) number K903718.

Who is the listed applicant for OROSCOPE MODEL NUMBER COS-100?

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

What is the FDA product code for OROSCOPE MODEL NUMBER COS-100?

The FDA product code for OROSCOPE MODEL NUMBER COS-100 is EHZ.

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 Cygnus Instruments, 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: EHZ)

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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