FDA 510(k) Premarket Notification K953018: UNI-SITE

Submission Details & Decision

Normalized public record details for 510(k) notification K953018.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K953018

Applicant / Sponsor

Ttl Medical

Device Name

UNI-SITE

Product Code

MGP

Decision Date

1995-09-08

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Unknown ()

Clearance Type

Traditional

Third Party Flag

Date Received

1995-06-29

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Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.