FDA 510(k)

PREPARED MUELLER HINTON MED/100 MM

K-Number: K833506 · 1983-12-01

Decision Date1983-12-01

Product CodeJTZ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

PREPARED MUELLER HINTON MED/100 MM is the device name listed in this FDA 510(k) record. The listed applicant is Lavco Laboratory, Inc.. It received FDA 510(k) clearance on 1983-12-01 under 510(k) number K833506. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREPARED MUELLER HINTON MED/100 MM?

PREPARED MUELLER HINTON MED/100 MM is a medical device that received FDA 510(k) clearance on 1983-12-01. The listed applicant is Lavco Laboratory, Inc.. The 510(k) number is K833506.

When did PREPARED MUELLER HINTON MED/100 MM receive FDA 510(k) clearance?

PREPARED MUELLER HINTON MED/100 MM received FDA 510(k) clearance on 1983-12-01, under 510(k) number K833506.

Who is the listed applicant for PREPARED MUELLER HINTON MED/100 MM?

The FDA 510(k) record lists Lavco Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREPARED MUELLER HINTON MED/100 MM?

The FDA product code for PREPARED MUELLER HINTON MED/100 MM is JTZ.

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Other records listing Lavco Laboratory, Inc. as applicant

K833507PREPARED TRYPTIC SOY AGAR 100 MM PLATE K833508PREPARED MACCONKEY AGAR

Related Devices (Code: JTZ)

K262163BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton BrothBecton Dickinson and Company K963036MUELLER HINTON II BROTH (CATION-ADJUSTED) WITH LYSED HORSE BLOODBecton Dickinson Microbiology Systems K960420MUELLER HINTON AGAR WITH 5% SHEEP BLOODBecton Dickinson Microbiology Systems K960313MUELLER HINTON AGAR WITH 2% NACIRemel, L.P.K945911CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARSBioclinical Systems, Inc.K941985MUELLER HINTON AGAR W/OXACILLINCarr-Scarborough Microbiologicals, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.