Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MINI MASH 2000

K-Number: K854602 · 1985-12-06

ApplicantDynatech Corp.
Decision Date1985-12-06
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINI MASH 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1985-12-06 under 510(k) number K854602. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI MASH 2000?

MINI MASH 2000 is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Dynatech Corp.. The 510(k) number is K854602.

When did MINI MASH 2000 receive FDA 510(k) clearance?

MINI MASH 2000 received FDA 510(k) clearance on 1985-12-06, under 510(k) number K854602.

Who is the listed applicant for MINI MASH 2000?

The FDA 510(k) record lists Dynatech Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI MASH 2000?

The FDA product code for MINI MASH 2000 is LIB.

Other records listing Dynatech Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K904567DYNATECH MR4000 MICROPLATE READERK854604AUTO MASHK854603MULTI MASH 2000K832117IMMULON SUBSTRATE REMOVAWELL STRIPSK823787HANDI-WASHK823833MICRO STIX #011-010-5000 & HOLDER#5100

View all 27 devices →

Related Devices (Code: LIB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K023677OSMETECH MICROBIAL ANALYSER-BACTERIAL VAGINOSIS (OMA-BV)OsmetechK920416SUPPLEMENTARY REAGENTS FOR ENZYGNOST/TMBBehring Diagnostics, Inc.K912558GULL ELISAWAREGull Laboratories, Inc.K872273CORNING EASY WASH ELISA PLATESCorning Medical & ScientificK871559CELL LIFTERCorning Costar Corp.K864249NORMAL SALINE STERILEMds Laboratories, Inc.

Official Source

View on FDA Database →

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

↑