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FDA 510(k)

TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE

K-Number: K901239 · 1990-05-15

ApplicantTeledyne Getz
Decision Date1990-05-15
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Getz. It received FDA 510(k) clearance on 1990-05-15 under 510(k) number K901239. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE?

TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Teledyne Getz. The 510(k) number is K901239.

When did TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?

TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1990-05-15, under 510(k) number K901239.

Who is the listed applicant for TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE?

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

What is the FDA product code for TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE?

The FDA product code for TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE is EFB.

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Other records listing Teledyne Getz 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.

K923674DENSPRO COARSE MINT PROPHY PASTEK923675DENSPRO MEDIUM MINT PROPHY PASTEK903568SUPER STRENGTH DENTURE ADHESIVE CREAMK901938SUPER STRENGTH DENTURE ADHESIVE CREAM

Related Devices (Code: EFB)

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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