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FDA 510(k)

FLOSER PLUS

K-Number: K884145 · 1988-10-19

ApplicantPacific Lin Intl., Co.
Decision Date1988-10-19
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Lin Intl., Co.. It received FDA 510(k) clearance on 1988-10-19 under 510(k) number K884145. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOSER PLUS?

FLOSER PLUS is a medical device that received FDA 510(k) clearance on 1988-10-19. The listed applicant is Pacific Lin Intl., Co.. The 510(k) number is K884145.

When did FLOSER PLUS receive FDA 510(k) clearance?

FLOSER PLUS received FDA 510(k) clearance on 1988-10-19, under 510(k) number K884145.

Who is the listed applicant for FLOSER PLUS?

The FDA 510(k) record lists Pacific Lin Intl., Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOSER PLUS?

The FDA product code for FLOSER PLUS is JES.

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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.

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