Cleared Traditional

K872916 - HISTOMATIC SLIDE STAINER, CODE-ON VERSION

K872916 is an FDA 510(k) clearance for HISTOMATIC SLIDE STAINER, manufactured by Fisher Scientific Co., LLC. The device is a Class 1 Hematology device with product code KPA cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K872916 · Fisher Scientific Co., LLC · Hematology device
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Sep 1987
Decision
52d
Days
Class 1
Risk

K872916 is an FDA 510(k) clearance for the HISTOMATIC SLIDE STAINER, CODE-ON VERSION. Classified as Slide Stainer, Automated (product code KPA), Class I - General Controls.

Submitted by Fisher Scientific Co., LLC (Indiana, US). The FDA issued a Cleared decision on September 14, 1987 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.3800 - the FDA hematology 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 Fisher Scientific Co., LLC devices

FDA 510(k) Submission Details - K872916

510(k) Number K872916 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1987
Decision Date September 14, 1987
Days to Decision 52 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 113d · This submission: 52d
Pathway characteristics
Predicate-based equivalence.

KPA Device Classification - Class 1, General Controls

Product Code KPA Slide Stainer, Automated
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.3800
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 - KPA Slide Stainer, Automated

All 9
Devices cleared under the same product code (KPA) and FDA review panel - the closest regulatory comparables to K872916.
LX-100 SLIDE STAINER
K880745 · Innovative Medical Systems, Inc. · Apr 1988
CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS
K850157 · Shaban Mfg. Co. · Feb 1985
PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERS
K850333 · Shaban Mfg. Co. · Feb 1985
MIDAS II AUTOMATIC STAINER
K842077 · Innovative Medical Systems, Inc. · Jul 1984
MIDAS 6000 AUTOMATIC STAINER
K832994 · Innovative Medical Systems, Inc. · Sep 1983
MI DAS 1000 AUTOMATIC SLIDE STAINER
K821830 · Innovative Medical Systems, Inc. · Jul 1982