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FDA 510(k)

1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

K-Number: K851720 · 1985-07-02

ApplicantArtiberia
Decision Date1985-07-02
Product CodeEGN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851720. The device is classified under product code EGN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS?

1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Artiberia. The 510(k) number is K851720.

When did 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS receive FDA 510(k) clearance?

1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851720.

Who is the listed applicant for 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS?

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 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS?

The FDA product code for 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS is EGN.

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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.

K8517451-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON BK85178627-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFK8517231300/10 TO 1305/89-92 VARIOUS CUTTING INSTRUMENTSK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES

View all 79 devices →

Related Devices (Code: EGN)

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.

K932675GXP DENTAL X-RAY PROCESSORGendex Corp.K821292TONSIL SCISSORS 7Conphar, Inc.K821275MAYO SCISSOR STRAIGHT 5 1/2Conphar, Inc.K821294TONSIL SCISSORS STRAIGHT 5 1/2Conphar, Inc.K821276MAYO SCISSOR CURYED 5 1/2Conphar, Inc.K821077CONPHARConphar, Inc.

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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