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FDA 510(k)

PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.

K-Number: K902268 · 1990-06-21

ApplicantSeabrook Medical Systems, Inc.
Decision Date1990-06-21
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM. is the device name listed in this FDA 510(k) record. The listed applicant is Seabrook Medical Systems, Inc.. It received FDA 510(k) clearance on 1990-06-21 under 510(k) number K902268. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.?

PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM. is a medical device that received FDA 510(k) clearance on 1990-06-21. The listed applicant is Seabrook Medical Systems, Inc.. The 510(k) number is K902268.

When did PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM. receive FDA 510(k) clearance?

PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM. received FDA 510(k) clearance on 1990-06-21, under 510(k) number K902268.

Who is the listed applicant for PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.?

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

What is the FDA product code for PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.?

The FDA product code for PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM. is ILO.

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Other records listing Seabrook Medical Systems, Inc. as applicant

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Related Devices (Code: ILO)

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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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