VERICORD S3
K-Number: K894123 · 1989-08-28
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Device Summary
Frequently Asked Questions
What is the VERICORD S3?
VERICORD S3 is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K894123.
When did VERICORD S3 receive FDA 510(k) clearance?
VERICORD S3 received FDA 510(k) clearance on 1989-08-28, under 510(k) number K894123.
Who is the listed applicant for VERICORD S3?
The FDA 510(k) record lists Philips Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERICORD S3?
The FDA product code for VERICORD S3 is IYE.
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 Philips Medical Systems, 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: IYE)
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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