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FDA 510(k)

1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE

K-Number: K850602 · 1985-04-25

ApplicantLife-Tech Intl., Inc.
Decision Date1985-04-25
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE 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 1985-04-25 under 510(k) number K850602. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE?

1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K850602.

When did 1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE receive FDA 510(k) clearance?

1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850602.

Who is the listed applicant for 1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE?

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 1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE?

The FDA product code for 1870T PRESSURE TRANSDUCER PRE-AMPLIFIER, 1880 WATE is FAP.

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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, PL150K955031MAXISTIMK954505EZ STIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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Related Devices (Code: FAP)

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.

K113771SIGNAL GEAR URETHRAL CATHETER ELECTRODENeurovision Medical Products, Inc.K974775SINGLE CHANNEL UROLOGICAL PRESSURE GAUGE, DUAL CHANNEL UROLOGICAL PRESSURE GAUGEAirtronic Services, Inc.K963330URODYNAMIC ANALYSIS MODULESynectics Medical, Inc.K962472RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETERRusch Intl.K931175SCHUSTER DISPOSABLE BALLOON PROBESandhill Scientific, Inc.K931179UROLAB SPECTRUMLife-Tech Intl., 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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