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)

THERADAPT HIGHCHAIR/STROLLER INSERT

K-Number: K942397 · 1994-06-22

Decision Date1994-06-22
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERADAPT HIGHCHAIR/STROLLER INSERT is the device name listed in this FDA 510(k) record. The listed applicant is Theradapt Products, Inc.. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K942397. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERADAPT HIGHCHAIR/STROLLER INSERT?

THERADAPT HIGHCHAIR/STROLLER INSERT is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Theradapt Products, Inc.. The 510(k) number is K942397.

When did THERADAPT HIGHCHAIR/STROLLER INSERT receive FDA 510(k) clearance?

THERADAPT HIGHCHAIR/STROLLER INSERT received FDA 510(k) clearance on 1994-06-22, under 510(k) number K942397.

Who is the listed applicant for THERADAPT HIGHCHAIR/STROLLER INSERT?

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

What is the FDA product code for THERADAPT HIGHCHAIR/STROLLER INSERT?

The FDA product code for THERADAPT HIGHCHAIR/STROLLER INSERT is INN.

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 Theradapt Products, 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.

Related Devices (Code: INN)

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.

↑