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FDA 510(k)

EPHAR

K-Number: K843214 · 1984-11-29

ApplicantAkron City Hospital
Decision Date1984-11-29
Product CodeFFI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EPHAR is the device name listed in this FDA 510(k) record. The listed applicant is Akron City Hospital. It received FDA 510(k) clearance on 1984-11-29 under 510(k) number K843214. The device is classified under product code FFI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPHAR?

EPHAR is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Akron City Hospital. The 510(k) number is K843214.

When did EPHAR receive FDA 510(k) clearance?

EPHAR received FDA 510(k) clearance on 1984-11-29, under 510(k) number K843214.

Who is the listed applicant for EPHAR?

The FDA 510(k) record lists Akron City Hospital as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPHAR?

The FDA product code for EPHAR is FFI.

Related Clinical Trials

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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Other records listing Akron City Hospital 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.

K853280FOUR CHANNEL PH PROBE

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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