POWERED VACUUM ASPIRATOR 1110-G-062
K-Number: K920288 · 1992-06-29
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Device Summary
Frequently Asked Questions
What is the POWERED VACUUM ASPIRATOR 1110-G-062?
POWERED VACUUM ASPIRATOR 1110-G-062 is a medical device that received FDA 510(k) clearance on 1992-06-29. The listed applicant is Stirn Industries. The 510(k) number is K920288.
When did POWERED VACUUM ASPIRATOR 1110-G-062 receive FDA 510(k) clearance?
POWERED VACUUM ASPIRATOR 1110-G-062 received FDA 510(k) clearance on 1992-06-29, under 510(k) number K920288.
Who is the listed applicant for POWERED VACUUM ASPIRATOR 1110-G-062?
The FDA 510(k) record lists Stirn Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWERED VACUUM ASPIRATOR 1110-G-062?
The FDA product code for POWERED VACUUM ASPIRATOR 1110-G-062 is JCX.
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 Stirn Industries 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: JCX)
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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