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FDA 510(k)

POWERED VACUUM ASPIRATOR 1110-G-062

K-Number: K920288 · 1992-06-29

Decision Date1992-06-29
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWERED VACUUM ASPIRATOR 1110-G-062 is the device name listed in this FDA 510(k) record. The listed applicant is Stirn Industries. It received FDA 510(k) clearance on 1992-06-29 under 510(k) number K920288. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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