FDA 510(k)

ECS 502

K-Number: K840717 · 1985-08-19

Decision Date1985-08-19

Product CodeDRT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ECS 502 is the device name listed in this FDA 510(k) record. The listed applicant is Robert Bosch Corp.. It received FDA 510(k) clearance on 1985-08-19 under 510(k) number K840717. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECS 502?

ECS 502 is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Robert Bosch Corp.. The 510(k) number is K840717.

When did ECS 502 receive FDA 510(k) clearance?

ECS 502 received FDA 510(k) clearance on 1985-08-19, under 510(k) number K840717.

Who is the listed applicant for ECS 502?

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

What is the FDA product code for ECS 502?

The FDA product code for ECS 502 is DRT.

Other records listing Robert Bosch Corp. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.