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FDA 510(k)

LACHRYMAL PROBES-VARIOUS

K-Number: K841002 · 1984-05-09

ApplicantPremier Dental Products Co.
Decision Date1984-05-09
Product CodeHNW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LACHRYMAL PROBES-VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841002. The device is classified under product code HNW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACHRYMAL PROBES-VARIOUS?

LACHRYMAL PROBES-VARIOUS is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Premier Dental Products Co.. The 510(k) number is K841002.

When did LACHRYMAL PROBES-VARIOUS receive FDA 510(k) clearance?

LACHRYMAL PROBES-VARIOUS received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841002.

Who is the listed applicant for LACHRYMAL PROBES-VARIOUS?

The FDA 510(k) record lists Premier Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LACHRYMAL PROBES-VARIOUS?

The FDA product code for LACHRYMAL PROBES-VARIOUS is HNW.

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Other records listing Premier Dental Products Co. 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.

K132526KNIT-PAK+K131212PREMIER CERAMIC PRIMERK083695TRAXODENTK062683ENAMEL PRO VARNISHK062166ENAMEL PROK061998PREMIER SELF-ETCHING BOND ENHANCER

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Related Devices (Code: HNW)

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.

K862070INTER-SHARPIntermedics Intraocular, Inc.K812097KOI LACREMAL HOOK & DILATORKoi, Inc.

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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