Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LEARN MODE WATERPROOF PENDANT PANIC BUTTON

K-Number: K940223 · 1994-04-29

Decision Date1994-04-29
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEARN MODE WATERPROOF PENDANT PANIC BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Interactive Technologies, Inc.. It received FDA 510(k) clearance on 1994-04-29 under 510(k) number K940223. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEARN MODE WATERPROOF PENDANT PANIC BUTTON?

LEARN MODE WATERPROOF PENDANT PANIC BUTTON is a medical device that received FDA 510(k) clearance on 1994-04-29. The listed applicant is Interactive Technologies, Inc.. The 510(k) number is K940223.

When did LEARN MODE WATERPROOF PENDANT PANIC BUTTON receive FDA 510(k) clearance?

LEARN MODE WATERPROOF PENDANT PANIC BUTTON received FDA 510(k) clearance on 1994-04-29, under 510(k) number K940223.

Who is the listed applicant for LEARN MODE WATERPROOF PENDANT PANIC BUTTON?

The FDA 510(k) record lists Interactive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEARN MODE WATERPROOF PENDANT PANIC BUTTON?

The FDA product code for LEARN MODE WATERPROOF PENDANT PANIC BUTTON is IQA.

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.

Related Devices (Code: IQA)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑