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FDA 510(k)

SALIVA EJECTOR

K-Number: K760620 · 1976-09-21

ApplicantLorvic Corp.
Decision Date1976-09-21
Product CodeDYN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SALIVA EJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Lorvic Corp.. It received FDA 510(k) clearance on 1976-09-21 under 510(k) number K760620. The device is classified under product code DYN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALIVA EJECTOR?

SALIVA EJECTOR is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is Lorvic Corp.. The 510(k) number is K760620.

When did SALIVA EJECTOR receive FDA 510(k) clearance?

SALIVA EJECTOR received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760620.

Who is the listed applicant for SALIVA EJECTOR?

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

What is the FDA product code for SALIVA EJECTOR?

The FDA product code for SALIVA EJECTOR is DYN.

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 Lorvic Corp. 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.

Related Devices (Code: DYN)

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

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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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