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FDA 510(k)

BOVO MOISTURE GUARD

K-Number: K850988 · 1985-04-16

ApplicantE.H. Medical Co.
Decision Date1985-04-16
Product CodeKHR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BOVO MOISTURE GUARD is the device name listed in this FDA 510(k) record. The listed applicant is E.H. Medical Co.. It received FDA 510(k) clearance on 1985-04-16 under 510(k) number K850988. The device is classified under product code KHR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOVO MOISTURE GUARD?

BOVO MOISTURE GUARD is a medical device that received FDA 510(k) clearance on 1985-04-16. The listed applicant is E.H. Medical Co.. The 510(k) number is K850988.

When did BOVO MOISTURE GUARD receive FDA 510(k) clearance?

BOVO MOISTURE GUARD received FDA 510(k) clearance on 1985-04-16, under 510(k) number K850988.

Who is the listed applicant for BOVO MOISTURE GUARD?

The FDA 510(k) record lists E.H. Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOVO MOISTURE GUARD?

The FDA product code for BOVO MOISTURE GUARD is KHR.

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Related Devices (Code: KHR)

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.

K980783SIMPLEX SALIVA ABSORBER/COLLECTOR, MODEL SSA-5Irt Management Corp.K954068GENERAL HYGIENE KITPhysician Industries, Inc.K953812GAUZE SPONGERemington Medical, Inc.K891054NON-STERILE GAUZE SPONGEDispomed, Inc.K891354ORTHODONTIC COTTON ROLL HOLDERSAmerican OrthodonticsK890734DRY TIPSMicrocopy, Div. Neo-Flo, 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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