CAVRO IQ-190 SAMPLE PROCESSOR
K-Number: K822208 · 1982-08-27
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Device Summary
Frequently Asked Questions
What is the CAVRO IQ-190 SAMPLE PROCESSOR?
CAVRO IQ-190 SAMPLE PROCESSOR is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Cavro Scientific Instruments, Inc.. The 510(k) number is K822208.
When did CAVRO IQ-190 SAMPLE PROCESSOR receive FDA 510(k) clearance?
CAVRO IQ-190 SAMPLE PROCESSOR received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822208.
Who is the listed applicant for CAVRO IQ-190 SAMPLE PROCESSOR?
The FDA 510(k) record lists Cavro Scientific Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAVRO IQ-190 SAMPLE PROCESSOR?
The FDA product code for CAVRO IQ-190 SAMPLE PROCESSOR is JQW.
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 Cavro Scientific 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: JQW)
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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