CARDIOVASCULAR INSTRUMENTS-VARIOUS
K-Number: K791710 · 1979-09-12
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Device Summary
Frequently Asked Questions
What is the CARDIOVASCULAR INSTRUMENTS-VARIOUS?
CARDIOVASCULAR INSTRUMENTS-VARIOUS is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791710.
When did CARDIOVASCULAR INSTRUMENTS-VARIOUS receive FDA 510(k) clearance?
CARDIOVASCULAR INSTRUMENTS-VARIOUS received FDA 510(k) clearance on 1979-09-12, under 510(k) number K791710.
Who is the listed applicant for CARDIOVASCULAR INSTRUMENTS-VARIOUS?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARDIOVASCULAR INSTRUMENTS-VARIOUS?
The FDA product code for CARDIOVASCULAR INSTRUMENTS-VARIOUS is DWS.
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 Edward Weck, 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: DWS)
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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