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FDA 510(k)

MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS

K-Number: K872039 · 1987-11-13

ApplicantLife-Tech Intl., Inc.
Decision Date1987-11-13
Product CodeEAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS 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 1987-11-13 under 510(k) number K872039. The device is classified under product code EAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS?

MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K872039.

When did MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS receive FDA 510(k) clearance?

MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS received FDA 510(k) clearance on 1987-11-13, under 510(k) number K872039.

Who is the listed applicant for MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS?

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 SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS?

The FDA product code for MODEL SK-14 STARTER KIT FOR DENTAL IONTOPHORESIS is EAT.

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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: EAT)

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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