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FDA 510(k)

7500 DATA TOWER

K-Number: K935498 · 1994-04-01

ApplicantE-Systems, Inc.
Decision Date1994-04-01
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

7500 DATA TOWER is the device name listed in this FDA 510(k) record. The listed applicant is E-Systems, Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K935498. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7500 DATA TOWER?

7500 DATA TOWER is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is E-Systems, Inc.. The 510(k) number is K935498.

When did 7500 DATA TOWER receive FDA 510(k) clearance?

7500 DATA TOWER received FDA 510(k) clearance on 1994-04-01, under 510(k) number K935498.

Who is the listed applicant for 7500 DATA TOWER?

The FDA 510(k) record lists E-Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 7500 DATA TOWER?

The FDA product code for 7500 DATA TOWER is LMB.

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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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