GSI 38 AUTO TYMP
K-Number: K925585 · 1993-02-02
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Device Summary
Frequently Asked Questions
What is the GSI 38 AUTO TYMP?
GSI 38 AUTO TYMP is a medical device that received FDA 510(k) clearance on 1993-02-02. The listed applicant is Lucas Grason-Stadler, Inc.. The 510(k) number is K925585.
When did GSI 38 AUTO TYMP receive FDA 510(k) clearance?
GSI 38 AUTO TYMP received FDA 510(k) clearance on 1993-02-02, under 510(k) number K925585.
Who is the listed applicant for GSI 38 AUTO TYMP?
The FDA 510(k) record lists Lucas Grason-Stadler, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GSI 38 AUTO TYMP?
The FDA product code for GSI 38 AUTO TYMP is ETY.
Other records listing Lucas Grason-Stadler, 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: ETY)
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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