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FDA 510(k)

Medline Digital Rectal Thermometer Sheath

K-Number: K183431 · 2019-06-14

ApplicantMedline Industries, Inc.
Decision Date2019-06-14
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Medline Digital Rectal Thermometer Sheath is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2019-06-14 under approval number K183431. 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 Medline Digital Rectal Thermometer Sheath?

Medline Digital Rectal Thermometer Sheath is a medical device that received FDA 510(k) clearance on 2019-06-14. It is manufactured by Medline Industries, Inc.. The 510(k) number is K183431.

When was Medline Digital Rectal Thermometer Sheath approved by the FDA?

Medline Digital Rectal Thermometer Sheath received FDA 510(k) clearance on 2019-06-14, under approval number K183431.

What company makes Medline Digital Rectal Thermometer Sheath?

Medline Digital Rectal Thermometer Sheath is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Digital Rectal Thermometer Sheath?

The FDA product code for Medline Digital Rectal Thermometer Sheath is FLL.

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Related Devices (Code: FLL)

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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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