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FDA 510(k)

TRANTECSILICONE QUARTZ DISP. TRANSD

K-Number: K833792 · 1984-02-10

ApplicantAmerican Bentley
Decision Date1984-02-10
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANTECSILICONE QUARTZ DISP. TRANSD is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K833792. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANTECSILICONE QUARTZ DISP. TRANSD?

TRANTECSILICONE QUARTZ DISP. TRANSD is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is American Bentley. The 510(k) number is K833792.

When did TRANTECSILICONE QUARTZ DISP. TRANSD receive FDA 510(k) clearance?

TRANTECSILICONE QUARTZ DISP. TRANSD received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833792.

Who is the listed applicant for TRANTECSILICONE QUARTZ DISP. TRANSD?

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

What is the FDA product code for TRANTECSILICONE QUARTZ DISP. TRANSD?

The FDA product code for TRANTECSILICONE QUARTZ DISP. TRANSD is DRS.

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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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