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FDA 510(k)

SENSOCOR TM R-TEST 24OXL

K-Number: K894234 · 1989-08-03

ApplicantSensocor
Decision Date1989-08-03
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SENSOCOR TM R-TEST 24OXL is the device name listed in this FDA 510(k) record. The listed applicant is Sensocor. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K894234. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOCOR TM R-TEST 24OXL?

SENSOCOR TM R-TEST 24OXL is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Sensocor. The 510(k) number is K894234.

When did SENSOCOR TM R-TEST 24OXL receive FDA 510(k) clearance?

SENSOCOR TM R-TEST 24OXL received FDA 510(k) clearance on 1989-08-03, under 510(k) number K894234.

Who is the listed applicant for SENSOCOR TM R-TEST 24OXL?

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

What is the FDA product code for SENSOCOR TM R-TEST 24OXL?

The FDA product code for SENSOCOR TM R-TEST 24OXL is DXG.

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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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