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FDA 510(k)

MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE

K-Number: K873206 · 1987-09-30

ApplicantRespiratory Support Products, Inc.
Decision Date1987-09-30
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1987-09-30 under 510(k) number K873206. The device is classified under product code DTW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE?

MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE is a medical device that received FDA 510(k) clearance on 1987-09-30. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K873206.

When did MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE receive FDA 510(k) clearance?

MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE received FDA 510(k) clearance on 1987-09-30, under 510(k) number K873206.

Who is the listed applicant for MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE?

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

What is the FDA product code for MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE?

The FDA product code for MYOCARDIAL TEMP. SENSOR W/TYPE T THERMOCOUPLE is DTW.

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Other records listing Respiratory Support Products, 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.

K983862CLOUD 1 HUMIDIFICATION SYSTEMK921190ADAP-TEMP TEMPERATURE SENSOR ADAPTERK920469MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIEK921510GAS SAMPLING KIT MODIFICATIONK913082BI-TEMP TEMPERATURE MONITOR,MODEL TM-300DK912280BI-TEMP TEMPERATURE MONITOR, MODEL TM-400D

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Related Devices (Code: DTW)

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.

K041558STOCKERTIR PURGE CONTROL (APC) SYSTEMStockert Instrumente GmbHK992857LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070Rocky Mountain Research, Inc.K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMERStoeckert InstrumenteK910599CARDIOPULMONARY BYPASS LEVEL SENSING MONITORJtl Medical Corp.K924354STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITORSorin Biomedica, Fiat, USA, Inc.K915337CAPIOX LEVEL ALARMTerumo Medical Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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