FDA 510(k)

RTM DVT PROSOFT CUFF MODEL NUMBER PS100

K-Number: K981643 · 1998-12-14

Decision Date1998-12-14

Product CodeJOW

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

RTM DVT PROSOFT CUFF MODEL NUMBER PS100 is the device name listed in this FDA 510(k) record. The listed applicant is R.T. Medical Services, Inc.. It received FDA 510(k) clearance on 1998-12-14 under 510(k) number K981643. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTM DVT PROSOFT CUFF MODEL NUMBER PS100?

RTM DVT PROSOFT CUFF MODEL NUMBER PS100 is a medical device that received FDA 510(k) clearance on 1998-12-14. The listed applicant is R.T. Medical Services, Inc.. The 510(k) number is K981643.

When did RTM DVT PROSOFT CUFF MODEL NUMBER PS100 receive FDA 510(k) clearance?

RTM DVT PROSOFT CUFF MODEL NUMBER PS100 received FDA 510(k) clearance on 1998-12-14, under 510(k) number K981643.

Who is the listed applicant for RTM DVT PROSOFT CUFF MODEL NUMBER PS100?

The FDA 510(k) record lists R.T. Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RTM DVT PROSOFT CUFF MODEL NUMBER PS100?

The FDA product code for RTM DVT PROSOFT CUFF MODEL NUMBER PS100 is JOW.

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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.