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FDA 510(k)

YANKAUER & POODLE SUCTION INSTRUMENTS

K-Number: K790419 · 1979-04-23

Decision Date1979-04-23
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YANKAUER & POODLE SUCTION INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Laboratories, Inc.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790419. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YANKAUER & POODLE SUCTION INSTRUMENTS?

YANKAUER & POODLE SUCTION INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K790419.

When did YANKAUER & POODLE SUCTION INSTRUMENTS receive FDA 510(k) clearance?

YANKAUER & POODLE SUCTION INSTRUMENTS received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790419.

Who is the listed applicant for YANKAUER & POODLE SUCTION INSTRUMENTS?

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

What is the FDA product code for YANKAUER & POODLE SUCTION INSTRUMENTS?

The FDA product code for YANKAUER & POODLE SUCTION INSTRUMENTS is BYY.

Related Clinical Trials

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.

Other records listing Snyder Laboratories, Inc. 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.

View all 16 devices →

Related Devices (Code: BYY)

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.

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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