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FDA 510(k)

PAM CARDIAC MONITOR

K-Number: K934684 · 1994-10-17

ApplicantTechnology Transfer, Inc.
Decision Date1994-10-17
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PAM CARDIAC MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Technology Transfer, Inc.. It received FDA 510(k) clearance on 1994-10-17 under 510(k) number K934684. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAM CARDIAC MONITOR?

PAM CARDIAC MONITOR is a medical device that received FDA 510(k) clearance on 1994-10-17. The listed applicant is Technology Transfer, Inc.. The 510(k) number is K934684.

When did PAM CARDIAC MONITOR receive FDA 510(k) clearance?

PAM CARDIAC MONITOR received FDA 510(k) clearance on 1994-10-17, under 510(k) number K934684.

Who is the listed applicant for PAM CARDIAC MONITOR?

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

What is the FDA product code for PAM CARDIAC MONITOR?

The FDA product code for PAM CARDIAC MONITOR is DRT.

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Related Devices (Code: DRT)

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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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