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FDA 510(k)

BETA/PAK

K-Number: K790769 · 1979-05-03

ApplicantBio/Data Corp.
Decision Date1979-05-03
Product CodeJOZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BETA/PAK 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 1979-05-03 under 510(k) number K790769. The device is classified under product code JOZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA/PAK?

BETA/PAK is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Bio/Data Corp.. The 510(k) number is K790769.

When did BETA/PAK receive FDA 510(k) clearance?

BETA/PAK received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790769.

Who is the listed applicant for BETA/PAK?

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 BETA/PAK?

The FDA product code for BETA/PAK is JOZ.

Other records listing Bio/Data Corp. as applicant

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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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