FDA 510(k)

SEA-BAND

K-Number: K033268 · 2004-01-07

Decision Date2004-01-07

Product CodeMVV

DecisionSubstantially Equivalent

Device Summary

SEA-BAND is the device name listed in this FDA 510(k) record. The listed applicant is Sea-Band UK , Ltd.. It received FDA 510(k) clearance on 2004-01-07 under 510(k) number K033268. The device is classified under product code MVV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEA-BAND?

SEA-BAND is a medical device that received FDA 510(k) clearance on 2004-01-07. The listed applicant is Sea-Band UK , Ltd.. The 510(k) number is K033268.

When did SEA-BAND receive FDA 510(k) clearance?

SEA-BAND received FDA 510(k) clearance on 2004-01-07, under 510(k) number K033268.

Who is the listed applicant for SEA-BAND?

The FDA 510(k) record lists Sea-Band UK , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEA-BAND?

The FDA product code for SEA-BAND is MVV.

Related Devices (Code: MVV)

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.

K220289FridaMom Anti-Nausea BandsFridababy, LLC K211823Bonine Acupressure BandsWellspring Pharmaceutical Corporation K193374TumEase Acupressure BraceletsMumease K110821BARF BANDDoodlebug Products, LLC K110563PRESSURE RIGHT, SINGLE-USE, DISPOSABLE, PRESSURE-SENSITIVE EMETIC-MANAGEMENT WRIST STRIPTherapeutics 101, Inc (Dba Pressure Point, Inc.)K070766PSI BANDSPsi Health Solutions, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.