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FDA 510(k)

POINTER F-3

K-Number: K833037 · 1983-11-29

ApplicantPetra Intl. Co.
Decision Date1983-11-29
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

POINTER F-3 is the device name listed in this FDA 510(k) record. The listed applicant is Petra Intl. Co.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K833037. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POINTER F-3?

POINTER F-3 is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Petra Intl. Co.. The 510(k) number is K833037.

When did POINTER F-3 receive FDA 510(k) clearance?

POINTER F-3 received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833037.

Who is the listed applicant for POINTER F-3?

The FDA 510(k) record lists Petra Intl. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POINTER F-3?

The FDA product code for POINTER F-3 is GZJ.

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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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