Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PULPDENT SNOOP

K-Number: K964430 · 1997-01-17

Decision Date1997-01-17
Product CodeLFC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PULPDENT SNOOP is the device name listed in this FDA 510(k) record. The listed applicant is Pulpdent Corp.. It received FDA 510(k) clearance on 1997-01-17 under 510(k) number K964430. The device is classified under product code LFC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULPDENT SNOOP?

PULPDENT SNOOP is a medical device that received FDA 510(k) clearance on 1997-01-17. The listed applicant is Pulpdent Corp.. The 510(k) number is K964430.

When did PULPDENT SNOOP receive FDA 510(k) clearance?

PULPDENT SNOOP received FDA 510(k) clearance on 1997-01-17, under 510(k) number K964430.

Who is the listed applicant for PULPDENT SNOOP?

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

What is the FDA product code for PULPDENT SNOOP?

The FDA product code for PULPDENT SNOOP is LFC.

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 Pulpdent 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.

View all 78 devices →

Related Devices (Code: LFC)

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.

↑