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FDA 510(k)

STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1

K-Number: K862510 · 1986-07-17

ApplicantShiley, Inc.
Decision Date1986-07-17
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1986-07-17 under 510(k) number K862510. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1?

STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Shiley, Inc.. The 510(k) number is K862510.

When did STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 receive FDA 510(k) clearance?

STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 received FDA 510(k) clearance on 1986-07-17, under 510(k) number K862510.

Who is the listed applicant for STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1?

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

What is the FDA product code for STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1?

The FDA product code for STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 is KRI.

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Other records listing Shiley, 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.

K920594SHILEY PERFUSION TUBING SETSK910991SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEMK911876SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200K910923BCD ADVANCEDK901548BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GASK903435SHILEY SPECIALIZED TRACHEOSTOMY TUBE

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Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, Inc.

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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