MINI SHOPPER
K-Number: K013927 · 2002-01-28
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Device Summary
Frequently Asked Questions
What is the MINI SHOPPER?
MINI SHOPPER is a medical device that received FDA 510(k) clearance on 2002-01-28. The listed applicant is Shoprider Intl., Inc.. The 510(k) number is K013927.
When did MINI SHOPPER receive FDA 510(k) clearance?
MINI SHOPPER received FDA 510(k) clearance on 2002-01-28, under 510(k) number K013927.
Who is the listed applicant for MINI SHOPPER?
The FDA 510(k) record lists Shoprider Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINI SHOPPER?
The FDA product code for MINI SHOPPER is INI.
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 Shoprider Intl., 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: INI)
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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