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FDA 510(k)

BET MODEL 1010

K-Number: K841000 · 1984-04-13

ApplicantBioelectro Technologies
Decision Date1984-04-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BET MODEL 1010 is the device name listed in this FDA 510(k) record. The listed applicant is Bioelectro Technologies. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K841000. 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 BET MODEL 1010?

BET MODEL 1010 is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Bioelectro Technologies. The 510(k) number is K841000.

When did BET MODEL 1010 receive FDA 510(k) clearance?

BET MODEL 1010 received FDA 510(k) clearance on 1984-04-13, under 510(k) number K841000.

Who is the listed applicant for BET MODEL 1010?

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

What is the FDA product code for BET MODEL 1010?

The FDA product code for BET MODEL 1010 is GZJ.

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Related Devices (Code: 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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