Cleared Traditional

K772210 - CULTURE COLLEC. TRANS. SYS.

K772210 is the FDA 510(k) clearance for CULTURE COLLEC. TRANS. SYS. by Precision Dynamics Corp.. It is a Class 1 Microbiology device (product code JTW) cleared through the Traditional 510(k) pathway after a 8-day FDA review.

K772210 · Precision Dynamics Corp. · Microbiology device
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Dec 1977
Decision
8d
Days
Class 1
Risk

K772210 is an FDA 510(k) clearance for the CULTURE COLLEC. TRANS. SYS., DOUBLE WET. Classified as System, Transport, Aerobic (product code JTW), Class I - General Controls.

Submitted by Precision Dynamics Corp. (Mchenry, US). The FDA issued a Cleared decision on December 9, 1977 after a review of 8 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2900 - the FDA microbiology device 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 Precision Dynamics Corp. devices

Submission Details

510(k) Number K772210 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 1977
Decision Date December 09, 1977
Days to Decision 8 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 102d · This submission: 8d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JTW System, Transport, Aerobic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2900
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 - JTW System, Transport, Aerobic

All 14
Devices cleared under the same product code (JTW) and FDA review panel - the closest regulatory comparables to K772210.
MINI-TIP CULTURETTE
K803298 · Marion Laboratories, Inc. · Jan 1981
URINE CULTURE KIT
K790366 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1979
CHAMBER, AEROBIC
K780440 · Marion Laboratories, Inc. · Apr 1978
EPTONE BACK-UP BROTH, VACUTAINER
K771058 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jul 1977
PEDIATRIC BLOOD CULTURE BOTTLES
K770957 · Gibco Laboratories Life Technologies, Inc. · Jun 1977
BOTTLE, BLOOD CULTURE, BI-PHASIC
K770683 · Gibco Laboratories Life Technologies, Inc. · Apr 1977