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FDA 510(k)

SUCTION DEVICE-PHARYNEAL DEVICE

K-Number: K840669 · 1984-06-11

Decision Date1984-06-11
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION DEVICE-PHARYNEAL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Lipsky-Dale Medical Products. It received FDA 510(k) clearance on 1984-06-11 under 510(k) number K840669. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION DEVICE-PHARYNEAL DEVICE?

SUCTION DEVICE-PHARYNEAL DEVICE is a medical device that received FDA 510(k) clearance on 1984-06-11. The listed applicant is Lipsky-Dale Medical Products. The 510(k) number is K840669.

When did SUCTION DEVICE-PHARYNEAL DEVICE receive FDA 510(k) clearance?

SUCTION DEVICE-PHARYNEAL DEVICE received FDA 510(k) clearance on 1984-06-11, under 510(k) number K840669.

Who is the listed applicant for SUCTION DEVICE-PHARYNEAL DEVICE?

The FDA 510(k) record lists Lipsky-Dale Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION DEVICE-PHARYNEAL DEVICE?

The FDA product code for SUCTION DEVICE-PHARYNEAL DEVICE is JOL.

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.

Related Devices (Code: JOL)

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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