MOTILITY GI MEDIUM
K-Number: K812798 · 1981-10-20
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Device Summary
Frequently Asked Questions
What is the MOTILITY GI MEDIUM?
MOTILITY GI MEDIUM is a medical device that received FDA 510(k) clearance on 1981-10-20. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K812798.
When did MOTILITY GI MEDIUM receive FDA 510(k) clearance?
MOTILITY GI MEDIUM received FDA 510(k) clearance on 1981-10-20, under 510(k) number K812798.
Who is the listed applicant for MOTILITY GI MEDIUM?
The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOTILITY GI MEDIUM?
The FDA product code for MOTILITY GI MEDIUM is JSG.
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 Isle Media and Sterile Products, 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: JSG)
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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