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FDA 510(k)

NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116

K-Number: K013133 · 2001-11-13

ApplicantNordix, Inc.
Decision Date2001-11-13
Product CodeMOQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 is the device name listed in this FDA 510(k) record. The listed applicant is Nordix, Inc.. It received FDA 510(k) clearance on 2001-11-13 under 510(k) number K013133. The device is classified under product code MOQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116?

NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 is a medical device that received FDA 510(k) clearance on 2001-11-13. The listed applicant is Nordix, Inc.. The 510(k) number is K013133.

When did NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 receive FDA 510(k) clearance?

NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 received FDA 510(k) clearance on 2001-11-13, under 510(k) number K013133.

Who is the listed applicant for NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116?

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

What is the FDA product code for NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116?

The FDA product code for NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 is MOQ.

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Related Devices (Code: MOQ)

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.

K081713VERTEBRAL ACCESS SYSTEM BY VIDACAREVidacare CorporationK980224ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822Alexander Mfg. Co.

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.

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