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FDA 510(k)

OBERTO MOUTH PROP

K-Number: K864962 · 1987-02-19

ApplicantMedovations, Inc.
Decision Date1987-02-19
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

OBERTO MOUTH PROP is the device name listed in this FDA 510(k) record. The listed applicant is Medovations, Inc.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K864962. The device is classified under product code JXL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBERTO MOUTH PROP?

OBERTO MOUTH PROP is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is Medovations, Inc.. The 510(k) number is K864962.

When did OBERTO MOUTH PROP receive FDA 510(k) clearance?

OBERTO MOUTH PROP received FDA 510(k) clearance on 1987-02-19, under 510(k) number K864962.

Who is the listed applicant for OBERTO MOUTH PROP?

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

What is the FDA product code for OBERTO MOUTH PROP?

The FDA product code for OBERTO MOUTH PROP is JXL.

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Other records listing Medovations, Inc. as applicant

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.

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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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