Cleared Traditional

K881716 - SCEPTOR - NEW ANTIMICROBIAL AGENT: CEFACLOR (FDA 510(k) Clearance)

Jul 1988
Decision
84d
Days
Class 2
Risk

K881716 is an FDA 510(k) clearance for the SCEPTOR - NEW ANTIMICROBIAL AGENT: CEFACLOR. This device is classified as a Manual Antimicrobial Susceptibility Test Systems (Class II - Special Controls, product code JWY).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lakes, US). The FDA issued a Cleared decision on July 14, 1988, 84 days after receiving the submission on April 21, 1988.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.1640.

Submission Details

510(k) Number K881716 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 21, 1988
Decision Date July 14, 1988
Days to Decision 84 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

Product Code JWY — Manual Antimicrobial Susceptibility Test Systems
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.1640

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