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FDA 510(k)

PILLING LACRIMAL INTUBATION SYSTEM

K-Number: K813187 · 1982-01-28

Decision Date1982-01-28
Product CodeHNL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PILLING LACRIMAL INTUBATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1982-01-28 under 510(k) number K813187. The device is classified under product code HNL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING LACRIMAL INTUBATION SYSTEM?

PILLING LACRIMAL INTUBATION SYSTEM is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is Narco Scientific. The 510(k) number is K813187.

When did PILLING LACRIMAL INTUBATION SYSTEM receive FDA 510(k) clearance?

PILLING LACRIMAL INTUBATION SYSTEM received FDA 510(k) clearance on 1982-01-28, under 510(k) number K813187.

Who is the listed applicant for PILLING LACRIMAL INTUBATION SYSTEM?

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

What is the FDA product code for PILLING LACRIMAL INTUBATION SYSTEM?

The FDA product code for PILLING LACRIMAL INTUBATION SYSTEM is HNL.

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 Narco Scientific 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 30 devices →

Related Devices (Code: HNL)

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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