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FDA 510(k)

DELFIA PLATE FLUOROMETER 1232

K-Number: K895240 · 1989-10-04

ApplicantPharmacia, Inc.
Decision Date1989-10-04
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DELFIA PLATE FLUOROMETER 1232 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1989-10-04 under 510(k) number K895240. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELFIA PLATE FLUOROMETER 1232?

DELFIA PLATE FLUOROMETER 1232 is a medical device that received FDA 510(k) clearance on 1989-10-04. The listed applicant is Pharmacia, Inc.. The 510(k) number is K895240.

When did DELFIA PLATE FLUOROMETER 1232 receive FDA 510(k) clearance?

DELFIA PLATE FLUOROMETER 1232 received FDA 510(k) clearance on 1989-10-04, under 510(k) number K895240.

Who is the listed applicant for DELFIA PLATE FLUOROMETER 1232?

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

What is the FDA product code for DELFIA PLATE FLUOROMETER 1232?

The FDA product code for DELFIA PLATE FLUOROMETER 1232 is KHO.

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Other records listing Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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Related Devices (Code: KHO)

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.

K112161AQT90 FLEX ANALYZER, AQT90 FLEX MYOGLOBIN TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LVLS 1-3, AQT90 FLEX MYO CAL CARTRIDGE..Radiometer Medical ApsK973547TRIAGE STATMETERBiosite IncorporatedK971103AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEMTosoh Medics, Inc.K962919VITROS IMMUNODIAGNOSTIC SYSTEMJohnson & Johnson Clinical Diagnostics, Inc.K952719BIOCIRCUITS IOS (IN-OFFICE SYSTEM)Biocircuits Corp.K950415FLUOROSCAN NEONATALIsolab, 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.

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