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FDA 510(k)

SUTURE NEEDLES

K-Number: K823229 · 1983-02-18

ApplicantFeuerstein Produktions
Decision Date1983-02-18
Product Code
DecisionSubstantially Equivalent

Device Summary

SUTURE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Feuerstein Produktions. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K823229. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE NEEDLES?

SUTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Feuerstein Produktions. The 510(k) number is K823229.

When did SUTURE NEEDLES receive FDA 510(k) clearance?

SUTURE NEEDLES received FDA 510(k) clearance on 1983-02-18, under 510(k) number K823229.

Who is the listed applicant for SUTURE NEEDLES?

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

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.

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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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