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)

NEEDLE NOSE PLIERS

K-Number: K864019 · 1986-10-30

Decision Date1986-10-30
Product CodeHTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEEDLE NOSE PLIERS is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tool, Inc.. It received FDA 510(k) clearance on 1986-10-30 under 510(k) number K864019. The device is classified under product code HTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE NOSE PLIERS?

NEEDLE NOSE PLIERS is a medical device that received FDA 510(k) clearance on 1986-10-30. The listed applicant is Med-Tool, Inc.. The 510(k) number is K864019.

When did NEEDLE NOSE PLIERS receive FDA 510(k) clearance?

NEEDLE NOSE PLIERS received FDA 510(k) clearance on 1986-10-30, under 510(k) number K864019.

Who is the listed applicant for NEEDLE NOSE PLIERS?

The FDA 510(k) record lists Med-Tool, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE NOSE PLIERS?

The FDA product code for NEEDLE NOSE PLIERS is HTC.

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 Med-Tool, Inc. 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 28 devices →

Related Devices (Code: HTC)

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.

↑