SECOND ASSISTANT
K-Number: K890501 · 1989-02-10
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Device Summary
Frequently Asked Questions
What is the SECOND ASSISTANT?
SECOND ASSISTANT is a medical device that received FDA 510(k) clearance on 1989-02-10. The listed applicant is 3M Company. The 510(k) number is K890501.
When did SECOND ASSISTANT receive FDA 510(k) clearance?
SECOND ASSISTANT received FDA 510(k) clearance on 1989-02-10, under 510(k) number K890501.
Who is the listed applicant for SECOND ASSISTANT?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECOND ASSISTANT?
The FDA product code for SECOND ASSISTANT is FWZ.
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 3M Company 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: FWZ)
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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