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FDA 510(k)

ACTIWATCH-SCORE

K-Number: K991033 · 1999-06-23

ApplicantMini-Mitter Co., Inc.
Decision Date1999-06-23
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACTIWATCH-SCORE is the device name listed in this FDA 510(k) record. The listed applicant is Mini-Mitter Co., Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991033. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIWATCH-SCORE?

ACTIWATCH-SCORE is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Mini-Mitter Co., Inc.. The 510(k) number is K991033.

When did ACTIWATCH-SCORE receive FDA 510(k) clearance?

ACTIWATCH-SCORE received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991033.

Who is the listed applicant for ACTIWATCH-SCORE?

The FDA 510(k) record lists Mini-Mitter Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTIWATCH-SCORE?

The FDA product code for ACTIWATCH-SCORE is GWQ.

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.

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Other records listing Mini-Mitter Co., 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.

K033534VITALSENSEK011430ACTIWARE-PLMSK991045MINI-LOGGER SERIES 2000K983533ACTIWATCH

Related Devices (Code: GWQ)

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.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

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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