FDA 510(k)

SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.

K-Number: K875063 · 1988-02-22

Decision Date1988-02-22

Product CodeHQG

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. is the device name listed in this FDA 510(k) record. The listed applicant is Epson EL Paso, Inc.. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K875063. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.?

SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Epson EL Paso, Inc.. The 510(k) number is K875063.

When did SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. receive FDA 510(k) clearance?

SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. received FDA 510(k) clearance on 1988-02-22, under 510(k) number K875063.

Who is the listed applicant for SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.?

The FDA 510(k) record lists Epson EL Paso, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.?

The FDA product code for SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. is HQG.

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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.