Cleared Traditional

ALPHA AMYLASE

K863052 · J. D. Assoc. · Chemistry
Sep 1986
Decision
28d
Days
Class 2
Risk

About This 510(k) Submission

K863052 is an FDA 510(k) clearance for the ALPHA AMYLASE, a Amyloclastic, Amylase (Class II — Special Controls, product code CJA), submitted by J. D. Assoc. (Montclair, US). The FDA issued a Cleared decision on September 9, 1986, 28 days after receiving the submission on August 12, 1986. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1070.

Submission Details

510(k) Number K863052 FDA.gov
FDA Decision Cleared SESE
Date Received August 12, 1986
Decision Date September 09, 1986
Days to Decision 28 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CJA — Amyloclastic, Amylase
Device Class Class II — Special Controls
CFR Regulation 21 CFR 862.1070

Similar Devices — CJA Amyloclastic, Amylase

All 9
MODIFIED HI CHEM AMYLASE REAGENT (PRODUCT #88129)
K895555 · Hichem Diagnostics · Dec 1989
AMYLASE REAGENT KIT FOR ASTRA SYSTEMS
K884226 · A-Kem, Inc. · Dec 1988
WAKO(TM) AUTOKIT AMYLASE
K883059 · Wako Chemicals USA, Inc. · Aug 1988
PARAMAX AMYLASE REAGENT
K873520 · Baxter Healthcare Corp · Nov 1987
AMYLASE LTS
K862640 · Electro-Nucleonics Laboratories, Inc. · Sep 1986
AMYLASE REAGENT SET (MODIFIED CARAWAY)
K860530 · Sterling Diagnostics, Inc. · Feb 1986