PERCEPTION SERIES DELIVERY SYS.
K-Number: K771890 · 1977-10-20
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Device Summary
Frequently Asked Questions
What is the PERCEPTION SERIES DELIVERY SYS.?
PERCEPTION SERIES DELIVERY SYS. is a medical device that received FDA 510(k) clearance on 1977-10-20. The listed applicant is Chayes Virginia, Inc.. The 510(k) number is K771890.
When did PERCEPTION SERIES DELIVERY SYS. receive FDA 510(k) clearance?
PERCEPTION SERIES DELIVERY SYS. received FDA 510(k) clearance on 1977-10-20, under 510(k) number K771890.
Who is the listed applicant for PERCEPTION SERIES DELIVERY SYS.?
The FDA 510(k) record lists Chayes Virginia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCEPTION SERIES DELIVERY SYS.?
The FDA product code for PERCEPTION SERIES DELIVERY SYS. is EIA.
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 Chayes Virginia, 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: EIA)
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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