RICA (DIAGNOSTIC INSTRUMENTS)
K-Number: K810054 · 1981-01-28
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Device Summary
Frequently Asked Questions
What is the RICA (DIAGNOSTIC INSTRUMENTS)?
RICA (DIAGNOSTIC INSTRUMENTS) is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Robert I. Chien & Assoc., Inc.. The 510(k) number is K810054.
When did RICA (DIAGNOSTIC INSTRUMENTS) receive FDA 510(k) clearance?
RICA (DIAGNOSTIC INSTRUMENTS) received FDA 510(k) clearance on 1981-01-28, under 510(k) number K810054.
Who is the listed applicant for RICA (DIAGNOSTIC INSTRUMENTS)?
The FDA 510(k) record lists Robert I. Chien & Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RICA (DIAGNOSTIC INSTRUMENTS)?
The FDA product code for RICA (DIAGNOSTIC INSTRUMENTS) is GWZ.
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 Robert I. Chien & Assoc., 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: GWZ)
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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