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)

LUO CURRETTES #3211

K-Number: K831119 · 1983-05-09

ApplicantPmt, Inc.
Decision Date1983-05-09
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LUO CURRETTES #3211 is the device name listed in this FDA 510(k) record. The listed applicant is Pmt, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K831119. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUO CURRETTES #3211?

LUO CURRETTES #3211 is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Pmt, Inc.. The 510(k) number is K831119.

When did LUO CURRETTES #3211 receive FDA 510(k) clearance?

LUO CURRETTES #3211 received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831119.

Who is the listed applicant for LUO CURRETTES #3211?

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

What is the FDA product code for LUO CURRETTES #3211?

The FDA product code for LUO CURRETTES #3211 is FZS.

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 Pmt, 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.

Related Devices (Code: FZS)

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.

↑