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FDA 510(k)

PROGRAMMABLE SPINAL CORAL STIM. SYSTEM

K-Number: K810182 · 1981-04-03

ApplicantElectronic Diagnostics, Inc.
Decision Date1981-04-03
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PROGRAMMABLE SPINAL CORAL STIM. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Diagnostics, Inc.. It received FDA 510(k) clearance on 1981-04-03 under 510(k) number K810182. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGRAMMABLE SPINAL CORAL STIM. SYSTEM?

PROGRAMMABLE SPINAL CORAL STIM. SYSTEM is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Electronic Diagnostics, Inc.. The 510(k) number is K810182.

When did PROGRAMMABLE SPINAL CORAL STIM. SYSTEM receive FDA 510(k) clearance?

PROGRAMMABLE SPINAL CORAL STIM. SYSTEM received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810182.

Who is the listed applicant for PROGRAMMABLE SPINAL CORAL STIM. SYSTEM?

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

What is the FDA product code for PROGRAMMABLE SPINAL CORAL STIM. SYSTEM?

The FDA product code for PROGRAMMABLE SPINAL CORAL STIM. SYSTEM is GZB.

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Official Source

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