ZIIP+ Device
K-Number: K212342 · 2021-09-23
Device Summary
Frequently Asked Questions
What is the ZIIP+ Device?
ZIIP+ Device is a medical device that received FDA 510(k) clearance on 2021-09-23. The listed applicant is Ziip, Inc.. The 510(k) number is K212342.
When did ZIIP+ Device receive FDA 510(k) clearance?
ZIIP+ Device received FDA 510(k) clearance on 2021-09-23, under 510(k) number K212342.
Who is the listed applicant for ZIIP+ Device?
The FDA 510(k) record lists Ziip, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZIIP+ Device?
The FDA product code for ZIIP+ Device is NFO.
Other records listing Ziip, 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: NFO)
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.