STONE DISLODGER
K-Number: K800608 · 1980-04-08
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Device Summary
Frequently Asked Questions
What is the STONE DISLODGER?
STONE DISLODGER is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is G.D. Searle and Co.. The 510(k) number is K800608.
When did STONE DISLODGER receive FDA 510(k) clearance?
STONE DISLODGER received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800608.
Who is the listed applicant for STONE DISLODGER?
The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STONE DISLODGER?
The FDA product code for STONE DISLODGER is FFL.
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 G.D. Searle and Co. 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: FFL)
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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