Cleared Traditional

NEYDIUM NPFLUX (FOR SOLDERING) (K770159) - FDA 510(k) Clearance

K770159 · Deringer-Ney, Inc. · Dental device
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Jan 1977
Decision
7d
Days
-
Risk

K770159 is an FDA 510(k) clearance for the NEYDIUM NPFLUX (FOR SOLDERING).

Submitted by Deringer-Ney, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 31, 1977 after a review of 7 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel. 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 Deringer-Ney, Inc. devices

Submission Details

510(k) Number K770159 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 1977
Decision Date January 31, 1977
Days to Decision 7 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
120d faster than avg
Panel avg: 127d · This submission: 7d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -