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FDA 510(k)

TURBOTRON 20/20

K-Number: K902920 · 1991-10-10

ApplicantPrestige Manufacturing Snd Bhd
Decision Date1991-10-10
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TURBOTRON 20/20 is the device name listed in this FDA 510(k) record. The listed applicant is Prestige Manufacturing Snd Bhd. It received FDA 510(k) clearance on 1991-10-10 under 510(k) number K902920. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBOTRON 20/20?

TURBOTRON 20/20 is a medical device that received FDA 510(k) clearance on 1991-10-10. The listed applicant is Prestige Manufacturing Snd Bhd. The 510(k) number is K902920.

When did TURBOTRON 20/20 receive FDA 510(k) clearance?

TURBOTRON 20/20 received FDA 510(k) clearance on 1991-10-10, under 510(k) number K902920.

Who is the listed applicant for TURBOTRON 20/20?

The FDA 510(k) record lists Prestige Manufacturing Snd Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURBOTRON 20/20?

The FDA product code for TURBOTRON 20/20 is LYL.

Related Clinical Trials

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Other records listing Prestige Manufacturing Snd Bhd as applicant

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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