Cleared Traditional

K851709 - 560 TO 577 VARIOUS TYPES OF FORCEPS FOR...

K851709 is an FDA 510(k) clearance for 560 TO 577 VARIOUS TYPES OF FORCEPS FOR..., manufactured by Artiberia. The device is a Class 1 Dental device with product code EMG cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K851709 · Artiberia · Dental device
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Jun 1985
Decision
47d
Days
Class 1
Risk

K851709 is an FDA 510(k) clearance for the 560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN. Classified as Forceps, Tooth Extractor, Surgical (product code EMG), Class I - General Controls.

Submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on June 11, 1985 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4565 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Artiberia devices

FDA 510(k) Submission Details - K851709

510(k) Number K851709 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1985
Decision Date June 11, 1985
Days to Decision 47 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 127d · This submission: 47d
Pathway characteristics
Predicate-based equivalence.

EMG Device Classification - Class 1, General Controls

Product Code EMG Forceps, Tooth Extractor, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4565
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EMG Forceps, Tooth Extractor, Surgical

Devices cleared under the same product code (EMG) and FDA review panel - the closest regulatory comparables to K851709.
500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA
K851708 · Artiberia · Jul 1985
600/7 TO 600/288 VARIOUS TYPES OF AMER. PATTERN DE
K851711 · Artiberia · Jun 1985
600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI
K851712 · Artiberia · Jun 1985
TOOTH EXTRACTING FORCEPS 151(2010)-875 PCS. SS410/
K851105 · The Huxley Instrument Corp. · May 1985
CAT. 8 DENTAL DEVICES
K840312 · Imm Enterprises , Ltd. · Apr 1984