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FDA 510(k)

VERONAL BUFFER

K-Number: K761171 · 1977-01-10

ApplicantBio/Data Corp.
Decision Date1977-01-10
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VERONAL BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Bio/Data Corp.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K761171. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERONAL BUFFER?

VERONAL BUFFER is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Bio/Data Corp.. The 510(k) number is K761171.

When did VERONAL BUFFER receive FDA 510(k) clearance?

VERONAL BUFFER received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761171.

Who is the listed applicant for VERONAL BUFFER?

The FDA 510(k) record lists Bio/Data Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERONAL BUFFER?

The FDA product code for VERONAL BUFFER is JPA.

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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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