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)

MIC-2000 QUAD INOCULUM TRAY

K-Number: K790971 · 1979-06-20

ApplicantDynatech Laboratories, Inc.
Decision Date1979-06-20
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIC-2000 QUAD INOCULUM TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1979-06-20 under 510(k) number K790971. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIC-2000 QUAD INOCULUM TRAY?

MIC-2000 QUAD INOCULUM TRAY is a medical device that received FDA 510(k) clearance on 1979-06-20. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K790971.

When did MIC-2000 QUAD INOCULUM TRAY receive FDA 510(k) clearance?

MIC-2000 QUAD INOCULUM TRAY received FDA 510(k) clearance on 1979-06-20, under 510(k) number K790971.

Who is the listed applicant for MIC-2000 QUAD INOCULUM TRAY?

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

What is the FDA product code for MIC-2000 QUAD INOCULUM TRAY?

The FDA product code for MIC-2000 QUAD INOCULUM TRAY is JTC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dynatech Laboratories, Inc. 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.

K962265MLX MICROTITER PLATE LUMINOMETERK934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)K943701MRX MICROPLATE READERK923456MICROLITE MICROTITER PLATE LUMINOMETER ML3000K915896MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODIK920888MICROLITE MICROTITER PLATE LUMINOMETER ML2200

View all 44 devices →

Related Devices (Code: JTC)

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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.

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.

↑