FDA 510(k)

BUFFER, CORNING MOPSO

K-Number: K790294 · 1979-03-21

Decision Date1979-03-21

Product CodeJHX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BUFFER, CORNING MOPSO is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790294. The device is classified under product code JHX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUFFER, CORNING MOPSO?

BUFFER, CORNING MOPSO is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Corning Medical & Scientific. The 510(k) number is K790294.

When did BUFFER, CORNING MOPSO receive FDA 510(k) clearance?

BUFFER, CORNING MOPSO received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790294.

Who is the listed applicant for BUFFER, CORNING MOPSO?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUFFER, CORNING MOPSO?

The FDA product code for BUFFER, CORNING MOPSO is JHX.

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Other records listing Corning Medical & Scientific as applicant

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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.