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FDA 510(k)

URINARY BLADDER TEMP. SENSOR #81-003

K-Number: K823077 · 1983-03-09

ApplicantClinical Technology Corp.
Decision Date1983-03-09
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

URINARY BLADDER TEMP. SENSOR #81-003 is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K823077. 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 URINARY BLADDER TEMP. SENSOR #81-003?

URINARY BLADDER TEMP. SENSOR #81-003 is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Clinical Technology Corp.. The 510(k) number is K823077.

When did URINARY BLADDER TEMP. SENSOR #81-003 receive FDA 510(k) clearance?

URINARY BLADDER TEMP. SENSOR #81-003 received FDA 510(k) clearance on 1983-03-09, under 510(k) number K823077.

Who is the listed applicant for URINARY BLADDER TEMP. SENSOR #81-003?

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

What is the FDA product code for URINARY BLADDER TEMP. SENSOR #81-003?

The FDA product code for URINARY BLADDER TEMP. SENSOR #81-003 is FLL.

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Other records listing Clinical Technology Corp. as applicant

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Related Devices (Code: FLL)

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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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