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FDA 510(k)

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD

K-Number: K863168 · 1986-10-24

Decision Date1986-10-24
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD 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 1986-10-24 under 510(k) number K863168. 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 MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD?

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K863168.

When did MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD receive FDA 510(k) clearance?

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863168.

Who is the listed applicant for MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD?

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 MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD?

The FDA product code for MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD is FAP.

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.

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.

View all 68 devices →

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.

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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