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FDA 510(k)

S&W ELECTRODE TYPES 888, 844, 988 AND 944

K-Number: K864586 · 1987-03-13

ApplicantS & W Medico Teknik
Decision Date1987-03-13
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

S&W ELECTRODE TYPES 888, 844, 988 AND 944 is the device name listed in this FDA 510(k) record. The listed applicant is S & W Medico Teknik. It received FDA 510(k) clearance on 1987-03-13 under 510(k) number K864586. 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 S&W ELECTRODE TYPES 888, 844, 988 AND 944?

S&W ELECTRODE TYPES 888, 844, 988 AND 944 is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is S & W Medico Teknik. The 510(k) number is K864586.

When did S&W ELECTRODE TYPES 888, 844, 988 AND 944 receive FDA 510(k) clearance?

S&W ELECTRODE TYPES 888, 844, 988 AND 944 received FDA 510(k) clearance on 1987-03-13, under 510(k) number K864586.

Who is the listed applicant for S&W ELECTRODE TYPES 888, 844, 988 AND 944?

The FDA 510(k) record lists S & W Medico Teknik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S&W ELECTRODE TYPES 888, 844, 988 AND 944?

The FDA product code for S&W ELECTRODE TYPES 888, 844, 988 AND 944 is DRX.

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Other records listing S & W Medico Teknik as applicant

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Related Devices (Code: 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.

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