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FDA 510(k)

MODEL T131 MEMORY TRANSMITTER

K-Number: K933021 · 1994-06-06

ApplicantBiometric Products, Inc.
Decision Date1994-06-06
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL T131 MEMORY TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Biometric Products, Inc.. It received FDA 510(k) clearance on 1994-06-06 under 510(k) number K933021. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL T131 MEMORY TRANSMITTER?

MODEL T131 MEMORY TRANSMITTER is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is Biometric Products, Inc.. The 510(k) number is K933021.

When did MODEL T131 MEMORY TRANSMITTER receive FDA 510(k) clearance?

MODEL T131 MEMORY TRANSMITTER received FDA 510(k) clearance on 1994-06-06, under 510(k) number K933021.

Who is the listed applicant for MODEL T131 MEMORY TRANSMITTER?

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

What is the FDA product code for MODEL T131 MEMORY TRANSMITTER?

The FDA product code for MODEL T131 MEMORY TRANSMITTER is DXH. This falls under the Hematology category.

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Other records listing Biometric Products, 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.

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Related Devices (Code: DXH)

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.

K250233PreemptiveAI Clinical SDKMeasure Labs, Inc. (Dba Preemptiveai, Inc.)K250258HeartBeam AIMIGo with 12-L ECG Synthesis Software SystemHeartbeam, Inc.K243438MEMO Patch M (MPT-E08R-UNC01)Huinno Co., Ltd.K243981Hexoskin Medical System (7100-00016)Carre Technologies, Inc.K243003VitalSigns 1-Lead Holter (VSH101)VitalSigns Technology Co., Ltd.K233521QT ECG (QTERD100)QT Medical, 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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