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)

PILLING K KNIFE

K-Number: K812918 · 1981-11-06

Decision Date1981-11-06
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PILLING K KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1981-11-06 under 510(k) number K812918. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING K KNIFE?

PILLING K KNIFE is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Narco Scientific. The 510(k) number is K812918.

When did PILLING K KNIFE receive FDA 510(k) clearance?

PILLING K KNIFE received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812918.

Who is the listed applicant for PILLING K KNIFE?

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 K KNIFE?

The FDA product code for PILLING K KNIFE is HNN.

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: HNN)

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.

↑