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FDA 510(k)

TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE)

K-Number: K902933 · 1990-08-23

ApplicantGeneral Electric Co.
Decision Date1990-08-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE) is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1990-08-23 under 510(k) number K902933. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE)?

TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE) is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is General Electric Co.. The 510(k) number is K902933.

When did TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE) receive FDA 510(k) clearance?

TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE) received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902933.

Who is the listed applicant for TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE)?

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

What is the FDA product code for TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE)?

The FDA product code for TESLACON (MAGNETIC RESONANCE DIAGNOSTIC DEVICE) is LNH.

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Other records listing General Electric Co. 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.

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