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FDA 510(k)

ACCUTEMP PLUS

K-Number: K881670 · 1988-11-22

ApplicantSentry Medical Products, Inc.
Decision Date1988-11-22
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCUTEMP PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Sentry Medical Products, Inc.. It received FDA 510(k) clearance on 1988-11-22 under 510(k) number K881670. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTEMP PLUS?

ACCUTEMP PLUS is a medical device that received FDA 510(k) clearance on 1988-11-22. The listed applicant is Sentry Medical Products, Inc.. The 510(k) number is K881670.

When did ACCUTEMP PLUS receive FDA 510(k) clearance?

ACCUTEMP PLUS received FDA 510(k) clearance on 1988-11-22, under 510(k) number K881670.

Who is the listed applicant for ACCUTEMP PLUS?

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

What is the FDA product code for ACCUTEMP PLUS?

The FDA product code for ACCUTEMP PLUS is FMT.

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Other records listing Sentry Medical Products, Inc. as applicant

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Related Devices (Code: FMT)

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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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