FDA 510(k)

SEAGER ELECTROEJACULATOR

K-Number: K962379 · 1997-09-18

Decision Date1997-09-18

Product CodeLNL

DecisionSubstantially Equivalent

Device Summary

SEAGER ELECTROEJACULATOR is the device name listed in this FDA 510(k) record. The listed applicant is National Rehab Hospital. It received FDA 510(k) clearance on 1997-09-18 under 510(k) number K962379. The device is classified under product code LNL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEAGER ELECTROEJACULATOR?

SEAGER ELECTROEJACULATOR is a medical device that received FDA 510(k) clearance on 1997-09-18. The listed applicant is National Rehab Hospital. The 510(k) number is K962379.

When did SEAGER ELECTROEJACULATOR receive FDA 510(k) clearance?

SEAGER ELECTROEJACULATOR received FDA 510(k) clearance on 1997-09-18, under 510(k) number K962379.

Who is the listed applicant for SEAGER ELECTROEJACULATOR?

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

What is the FDA product code for SEAGER ELECTROEJACULATOR?

The FDA product code for SEAGER ELECTROEJACULATOR is LNL.

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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.