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FDA 510(k)

ARANTROL

K-Number: K780835 · 1978-06-22

ApplicantAranco Diagnostic Laboratories, Inc.
Decision Date1978-06-22
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ARANTROL is the device name listed in this FDA 510(k) record. The listed applicant is Aranco Diagnostic Laboratories, Inc.. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780835. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARANTROL?

ARANTROL is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Aranco Diagnostic Laboratories, Inc.. The 510(k) number is K780835.

When did ARANTROL receive FDA 510(k) clearance?

ARANTROL received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780835.

Who is the listed applicant for ARANTROL?

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

What is the FDA product code for ARANTROL?

The FDA product code for ARANTROL is JPK.

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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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