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)

ADJUSTABLE TREATMENT TABLES

K-Number: K851690 · 1985-05-07

ApplicantI-Rep, Inc.
Decision Date1985-05-07
Product Code
DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE TREATMENT TABLES is the device name listed in this FDA 510(k) record. The listed applicant is I-Rep, Inc.. It received FDA 510(k) clearance on 1985-05-07 under 510(k) number K851690. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUSTABLE TREATMENT TABLES?

ADJUSTABLE TREATMENT TABLES is a medical device that received FDA 510(k) clearance on 1985-05-07. The listed applicant is I-Rep, Inc.. The 510(k) number is K851690.

When did ADJUSTABLE TREATMENT TABLES receive FDA 510(k) clearance?

ADJUSTABLE TREATMENT TABLES received FDA 510(k) clearance on 1985-05-07, under 510(k) number K851690.

Who is the listed applicant for ADJUSTABLE TREATMENT TABLES?

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

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 I-Rep, 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 8 devices →

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.

↑