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FDA 510(k)

560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN

K-Number: K851709 · 1985-06-11

ApplicantArtiberia
Decision Date1985-06-11
Product CodeEMG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K851709. The device is classified under product code EMG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN?

560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Artiberia. The 510(k) number is K851709.

When did 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN receive FDA 510(k) clearance?

560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851709.

Who is the listed applicant for 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN?

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

What is the FDA product code for 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN?

The FDA product code for 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN is EMG.

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 Artiberia 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 79 devices →

Related Devices (Code: EMG)

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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