FDA 510(k)

CVS Health 건조한 입喷雾, OraLabs 건조한 입喷雾

K-번호: K181839 · 2019-11-21

결정일2019-11-21

제품 코드LFD

결정대체적으로 동일

기기 요약

CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray is the device name listed in this FDA 510(k) record. The listed applicant is Oralabs, Inc.. It received FDA 510(k) clearance on 2019-11-21 under 510(k) number K181839. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?

CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray is a medical device that received FDA 510(k) clearance on 2019-11-21. The listed applicant is Oralabs, Inc.. The 510(k) number is K181839.

When did CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray receive FDA 510(k) clearance?

CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray received FDA 510(k) clearance on 2019-11-21, under 510(k) number K181839.

Who is the listed applicant for CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?

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

What is the FDA product code for CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?

The FDA product code for CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray is LFD.

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CVS Health 건조한 입喷雾, OraLabs 건조한 입喷雾

기기 요약

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관련 임상시험

관련 기기 (코드: LFD)

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