Cleared Traditional

K781283 - READER, INOCULUM, STDIZED. (FDA 510(k) Clearance)

K781283 · Analytical Products, Inc. · Microbiology device
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Aug 1978
Decision
19d
Days
-
Risk

K781283 is an FDA 510(k) clearance for the READER, INOCULUM, STDIZED..

Submitted by Analytical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 14, 1978 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Microbiology 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 Analytical Products, Inc. devices

Submission Details

510(k) Number K781283 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 26, 1978
Decision Date August 14, 1978
Days to Decision 19 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
83d faster than avg
Panel avg: 102d · This submission: 19d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -