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FDA 510(k)

IDEAL Ziploop

K-Number: K233552 · 2023-11-30

Decision Date2023-11-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IDEAL Ziploop is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2023-11-30 under 510(k) number K233552. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDEAL Ziploop?

IDEAL Ziploop is a medical device that received FDA 510(k) clearance on 2023-11-30. The listed applicant is Riverpoint Medical. The 510(k) number is K233552.

When did IDEAL Ziploop receive FDA 510(k) clearance?

IDEAL Ziploop received FDA 510(k) clearance on 2023-11-30, under 510(k) number K233552.

Who is the listed applicant for IDEAL Ziploop?

The FDA 510(k) record lists Riverpoint Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDEAL Ziploop?

The FDA product code for IDEAL Ziploop is MBI.

Other records listing Riverpoint Medical 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.

View all 30 devices →

Related Devices (Code: MBI)

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.