OROSCOPE MODEL NUMBER COS-100
K-Number: K903718 · 1990-11-09
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Device Summary
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
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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