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FDA 510(k)

MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE

K-Number: K920469 · 1992-09-11

Decision Date1992-09-11
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE 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 1992-09-11 under 510(k) number K920469. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE?

MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K920469.

When did MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE receive FDA 510(k) clearance?

MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE received FDA 510(k) clearance on 1992-09-11, under 510(k) number K920469.

Who is the listed applicant for MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE?

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 MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE?

The FDA product code for MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIE is FLL.

Related Clinical Trials

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.

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.

View all 27 devices →

Related Devices (Code: FLL)

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.

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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