FDA 510(k)

GDC PATIENT RETURN ELECTTRODE MODEL 45021

K-Number: K963307 · 1996-12-17

Decision Date1996-12-17

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

GDC PATIENT RETURN ELECTTRODE MODEL 45021 is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1996-12-17 under 510(k) number K963307. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GDC PATIENT RETURN ELECTTRODE MODEL 45021?

GDC PATIENT RETURN ELECTTRODE MODEL 45021 is a medical device that received FDA 510(k) clearance on 1996-12-17. The listed applicant is Target Therapeutics. The 510(k) number is K963307.

When did GDC PATIENT RETURN ELECTTRODE MODEL 45021 receive FDA 510(k) clearance?

GDC PATIENT RETURN ELECTTRODE MODEL 45021 received FDA 510(k) clearance on 1996-12-17, under 510(k) number K963307.

Who is the listed applicant for GDC PATIENT RETURN ELECTTRODE MODEL 45021?

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

What is the FDA product code for GDC PATIENT RETURN ELECTTRODE MODEL 45021?

The FDA product code for GDC PATIENT RETURN ELECTTRODE MODEL 45021 is HCG.

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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.