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FDA 510(k)

MEDITRODE KIT

K-Number: K882554 · 1988-12-23

ApplicantLife-Tech Intl., Inc.
Decision Date1988-12-23
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

MEDITRODE KIT 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 1988-12-23 under 510(k) number K882554. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDITRODE KIT?

MEDITRODE KIT is a medical device that received FDA 510(k) clearance on 1988-12-23. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K882554.

When did MEDITRODE KIT receive FDA 510(k) clearance?

MEDITRODE KIT received FDA 510(k) clearance on 1988-12-23, under 510(k) number K882554.

Who is the listed applicant for MEDITRODE KIT?

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 MEDITRODE KIT?

The FDA product code for MEDITRODE KIT is EGJ.

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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: EGJ)

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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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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