FDA 510(k)

VXTRA BACK PACK EKG ELECTRODE CAT. NO.

K-Number: K792436 · 1980-02-22

Decision Date1980-02-22

Product CodeDRX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VXTRA BACK PACK EKG ELECTRODE CAT. NO. is the device name listed in this FDA 510(k) record. The listed applicant is Vxtra Corp.. It received FDA 510(k) clearance on 1980-02-22 under 510(k) number K792436. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VXTRA BACK PACK EKG ELECTRODE CAT. NO.?

VXTRA BACK PACK EKG ELECTRODE CAT. NO. is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is Vxtra Corp.. The 510(k) number is K792436.

When did VXTRA BACK PACK EKG ELECTRODE CAT. NO. receive FDA 510(k) clearance?

VXTRA BACK PACK EKG ELECTRODE CAT. NO. received FDA 510(k) clearance on 1980-02-22, under 510(k) number K792436.

Who is the listed applicant for VXTRA BACK PACK EKG ELECTRODE CAT. NO.?

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

What is the FDA product code for VXTRA BACK PACK EKG ELECTRODE CAT. NO.?

The FDA product code for VXTRA BACK PACK EKG ELECTRODE CAT. NO. is DRX.

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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.