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FDA 510(k)

ESB 2400 SEI

K-Number: K933146 · 1993-09-23

ApplicantEsb, Inc., Div. of Ray-O-Vac
Decision Date1993-09-23
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ESB 2400 SEI is the device name listed in this FDA 510(k) record. The listed applicant is Esb, Inc., Div. of Ray-O-Vac. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K933146. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESB 2400 SEI?

ESB 2400 SEI is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Esb, Inc., Div. of Ray-O-Vac. The 510(k) number is K933146.

When did ESB 2400 SEI receive FDA 510(k) clearance?

ESB 2400 SEI received FDA 510(k) clearance on 1993-09-23, under 510(k) number K933146.

Who is the listed applicant for ESB 2400 SEI?

The FDA 510(k) record lists Esb, Inc., Div. of Ray-O-Vac as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESB 2400 SEI?

The FDA product code for ESB 2400 SEI is FTC.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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