INTRODUCERS
K-Number: K790034 · 1979-02-01
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Device Summary
Frequently Asked Questions
What is the INTRODUCERS?
INTRODUCERS is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Clincal Instruments Corp.. The 510(k) number is K790034.
When did INTRODUCERS receive FDA 510(k) clearance?
INTRODUCERS received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790034.
Who is the listed applicant for INTRODUCERS?
The FDA 510(k) record lists Clincal Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRODUCERS?
The FDA product code for INTRODUCERS is DYB.
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 Clincal Instruments Corp. 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: DYB)
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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