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FDA 510(k)

SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT

K-Number: K973176 · 1997-11-21

ApplicantLotus Technologies
Decision Date1997-11-21
Product CodeKGA
DecisionUnknown

Device Summary

SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Lotus Technologies. It received FDA 510(k) clearance on 1997-11-21 under 510(k) number K973176. The device is classified under product code KGA. FDA Decision: Unknown.

Frequently Asked Questions

What is the SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT?

SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT is a medical device that received FDA 510(k) clearance on 1997-11-21. The listed applicant is Lotus Technologies. The 510(k) number is K973176.

When did SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT receive FDA 510(k) clearance?

SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT received FDA 510(k) clearance on 1997-11-21, under 510(k) number K973176.

Who is the listed applicant for SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT?

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

What is the FDA product code for SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT?

The FDA product code for SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT is KGA.

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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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