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)

1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE

K-Number: K851748 · 1985-06-13

ApplicantArtiberia
Decision Date1985-06-13
Product CodeGWZ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-13 under 510(k) number K851748. The device is classified under product code GWZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE?

1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE is a medical device that received FDA 510(k) clearance on 1985-06-13. The listed applicant is Artiberia. The 510(k) number is K851748.

When did 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE receive FDA 510(k) clearance?

1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE received FDA 510(k) clearance on 1985-06-13, under 510(k) number K851748.

Who is the listed applicant for 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE?

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 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE?

The FDA product code for 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE is GWZ.

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: GWZ)

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.

↑