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FDA 510(k)

TUMISENSOR 1524

K-Number: K831251 · 1983-06-03

ApplicantLife-Tech Intl., Inc.
Decision Date1983-06-03
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

TUMISENSOR 1524 is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K831251. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUMISENSOR 1524?

TUMISENSOR 1524 is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K831251.

When did TUMISENSOR 1524 receive FDA 510(k) clearance?

TUMISENSOR 1524 received FDA 510(k) clearance on 1983-06-03, under 510(k) number K831251.

Who is the listed applicant for TUMISENSOR 1524?

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

What is the FDA product code for TUMISENSOR 1524?

The FDA product code for TUMISENSOR 1524 is LIL.

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Other records listing Life-Tech Intl., 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.

K001129PROLONG, MODELS PL50, PL100, PL150K954505EZ STIMK955031MAXISTIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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Related Devices (Code: LIL)

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.

K061676RIGIDOMETER, MODEL DIR-4UUroan 21K062042PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)Plethora SolutionsK052929PREFTEST PROFESSIONAL SUITELimestone Technologies, Inc.K033126MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEMBehavioral Technology, Inc.K000194DIGITAL INFLECTION RIGIDOMETER (DIR)Uroan Xxi ElectromedicinaK991479VISER PENILE TUMESCENCE MONITORLaborie Medical Tech 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.

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