Cleared Traditional

K832708 - PARAMAX CALCIUM REAGENT-GLUTAMY-TRANS

K832708 is the FDA 510(k) clearance for PARAMAX CALCIUM REAGENT-GLUTAMY-TRANS by American Dade. It is a Class 2 Chemistry device (product code CIC) cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K832708 · American Dade · Chemistry device
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Oct 1983
Decision
63d
Days
Class 2
Risk

K832708 is an FDA 510(k) clearance for the PARAMAX CALCIUM REAGENT-GLUTAMY-TRANS. Classified as Cresolphthalein Complexone, Calcium (product code CIC), Class II - Special Controls.

Submitted by American Dade (Mchenry, US). The FDA issued a Cleared decision on October 14, 1983 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1145 - the FDA in vitro diagnostics and chemistry 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 American Dade devices

Submission Details

510(k) Number K832708 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 1983
Decision Date October 14, 1983
Days to Decision 63 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d faster than avg
Panel avg: 88d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIC Cresolphthalein Complexone, Calcium
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1145
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 Chemistry devices follow this clearance model.

Regulatory Peers - CIC Cresolphthalein Complexone, Calcium

All 67
Devices cleared under the same product code (CIC) and FDA review panel - the closest regulatory comparables to K832708.
SERUM CALCIUM REAGENT SET
K841051 · Medical Specialties, Inc. · May 1984
FLOW-PAC CALCIUM REAGENT SET
K834336 · American Research Products Co. · Feb 1984
CALCIUM DYE REAGENT-CS-718-A/BUFFER
K833035 · Fisher Scientific Co., LLC · Nov 1983
ULTRA CHEM CRESOLCAVERSACHEM #65082
K830238 · Emd Chemicals, Inc. · Feb 1983
COBAS REAGENT FOR CALCIUM
K823577 · Hoffmann-La Roche, Inc. · Jan 1983
LIQUIZYME CALCIUM REAGENT SET
K823219 · American Research Products Co. · Dec 1982