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Data / Medical devices / Japan / MEDICAL & BIOLOGICAL LABORATORIES CO., LTD. Ina Laboratory

MEDICAL & BIOLOGICAL LABORATORIES CO., LTD. Ina Laboratory: FDA-registered device maker in INA Nagano, Japan, 1 510(k) clearance

MEDICAL & BIOLOGICAL LABORATORIES CO., LTD. Ina Laboratory is registered with the FDA (registration 3003155207) in INA Nagano, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 25, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003155207
Address
1018-1 Terasawaoka, INA Nagano, Japan, 396-0002
Owner or operator
MEDICAL & BIOLOGICAL LABORATORIES CO., LTD. Ina Laboratory (9039476)
Roles
Manufacturer
First device listed
December 16, 2008
Registered through
2026
Brand names listed
MESACUP BP180 ELISA Kit and MESACUP BP230 ELISA Kit

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 25, 2008K071961MESACUP MODELS BP180 AND BP230 ELISA KITSOEGSubstantially EquivalentMbl International Corporationaccessdata.fda.gov

Compare with other makers

Updated August 25, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.