Cleared Traditional

K813395 - CELLULOSE ACETATE-CITRATE AGAR HEMOGLO

K813395 is an FDA 510(k) clearance for CELLULOSE ACETATE-CITRATE AGAR HEMOGLO, manufactured by Helena Laboratories. The device is a Class 2 Microbiology device with product code JBD cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K813395 · Helena Laboratories · Microbiology device
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Dec 1981
Decision
27d
Days
Class 2
Risk

K813395 is an FDA 510(k) clearance for the CELLULOSE ACETATE-CITRATE AGAR HEMOGLO. Classified as System, Analysis, Electrophoretic Hemoglobin (product code JBD), Class II - Special Controls.

Submitted by Helena Laboratories (Walker, US). The FDA issued a Cleared decision on December 31, 1981 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 864.7440 - 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 Helena Laboratories devices

FDA 510(k) Submission Details - K813395

510(k) Number K813395 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 04, 1981
Decision Date December 31, 1981
Days to Decision 27 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 102d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JBD Device Classification - Class 2, Special Controls

Product Code JBD System, Analysis, Electrophoretic Hemoglobin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7440
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Microbiology devices follow this clearance model.

Regulatory Peers - JBD System, Analysis, Electrophoretic Hemoglobin

All 23
Devices cleared under the same product code (JBD) and FDA review panel - the closest regulatory comparables to K813395.
REP HEMOGLOBIN IEF KITS (CAT. NO. 3250)
K901143 · Helena Laboratories · May 1990
LABILE REMOVING HEMOLYZING REAGENT
K830804 · Corning Medical & Scientific · May 1983
GELMAN GLYCO-PHORE BUFFER
K820518 · Gelman Sciences, Inc. · Apr 1982
HEMOGLOBIN ELECTROPHORESIS CONTROL
K810919 · Isolab, Inc. · Apr 1981
AUTOPHOR 128
K810047 · Gelman Sciences, Inc. · Feb 1981
CORNING NORMAL GLYCOSYLATED HEMOGLOBIN
K802884 · Corning Medical & Scientific · Dec 1980