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FDA 510(k)

HEMAFLOUR ZP

K-Number: K760506 · 1976-10-28

ApplicantBuchler Instruments, Inc.
Decision Date1976-10-28
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HEMAFLOUR ZP is the device name listed in this FDA 510(k) record. The listed applicant is Buchler Instruments, Inc.. It received FDA 510(k) clearance on 1976-10-28 under 510(k) number K760506. 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 HEMAFLOUR ZP?

HEMAFLOUR ZP is a medical device that received FDA 510(k) clearance on 1976-10-28. The listed applicant is Buchler Instruments, Inc.. The 510(k) number is K760506.

When did HEMAFLOUR ZP receive FDA 510(k) clearance?

HEMAFLOUR ZP received FDA 510(k) clearance on 1976-10-28, under 510(k) number K760506.

Who is the listed applicant for HEMAFLOUR ZP?

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

What is the FDA product code for HEMAFLOUR ZP?

The FDA product code for HEMAFLOUR ZP is KHO.

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.

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Other records listing Buchler Instruments, 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.

K791312CATALOG #4-2520 CHLORIDOMETER CHLORIDE

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

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

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