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FDA 510(k)

JOVI MYELOGRAPHY HARNESS

K-Number: K872468 · 1987-07-01

ApplicantJovi, Inc.
Decision Date1987-07-01
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JOVI MYELOGRAPHY HARNESS is the device name listed in this FDA 510(k) record. The listed applicant is Jovi, Inc.. It received FDA 510(k) clearance on 1987-07-01 under 510(k) number K872468. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOVI MYELOGRAPHY HARNESS?

JOVI MYELOGRAPHY HARNESS is a medical device that received FDA 510(k) clearance on 1987-07-01. The listed applicant is Jovi, Inc.. The 510(k) number is K872468.

When did JOVI MYELOGRAPHY HARNESS receive FDA 510(k) clearance?

JOVI MYELOGRAPHY HARNESS received FDA 510(k) clearance on 1987-07-01, under 510(k) number K872468.

Who is the listed applicant for JOVI MYELOGRAPHY HARNESS?

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

What is the FDA product code for JOVI MYELOGRAPHY HARNESS?

The FDA product code for JOVI MYELOGRAPHY HARNESS is KPR.

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Related Devices (Code: KPR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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