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FDA 510(k)

ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE

K-Number: K801802 · 1981-01-02

ApplicantMedical Testing System, Inc.
Decision Date1981-01-02
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Testing System, Inc.. It received FDA 510(k) clearance on 1981-01-02 under 510(k) number K801802. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE?

ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE is a medical device that received FDA 510(k) clearance on 1981-01-02. The listed applicant is Medical Testing System, Inc.. The 510(k) number is K801802.

When did ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE receive FDA 510(k) clearance?

ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE received FDA 510(k) clearance on 1981-01-02, under 510(k) number K801802.

Who is the listed applicant for ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE?

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

What is the FDA product code for ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE?

The FDA product code for ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE is DPW.

Related Clinical Trials

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Other records listing Medical Testing System, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K801799ATRIAL/VENTRICULAR SEQENTIAL #080-20000K801800UNIVERSAL TEMP. PACING ELECT. #080-10000K791797MTS CATHETER ADAPTER FOR GUIDANCE ENTRYK770641MINI-CONER TM

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Official Source

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