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FDA 510(k)

HAKIM PROGRAMMER AND TRANSMITTER

K-Number: K003564 · 2000-12-20

Decision Date2000-12-20
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HAKIM PROGRAMMER AND TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 2000-12-20 under 510(k) number K003564. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAKIM PROGRAMMER AND TRANSMITTER?

HAKIM PROGRAMMER AND TRANSMITTER is a medical device that received FDA 510(k) clearance on 2000-12-20. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K003564.

When did HAKIM PROGRAMMER AND TRANSMITTER receive FDA 510(k) clearance?

HAKIM PROGRAMMER AND TRANSMITTER received FDA 510(k) clearance on 2000-12-20, under 510(k) number K003564.

Who is the listed applicant for HAKIM PROGRAMMER AND TRANSMITTER?

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

What is the FDA product code for HAKIM PROGRAMMER AND TRANSMITTER?

The FDA product code for HAKIM PROGRAMMER AND TRANSMITTER is JXG.

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.

Other records listing Codman & Shurtleff, 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.

View all 147 devices →

Related Devices (Code: JXG)

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.

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