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)

ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES

K-Number: K935157 · 1994-08-09

Decision Date1994-08-09
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Regulatory Consultants TO the Medical Device Indus. It received FDA 510(k) clearance on 1994-08-09 under 510(k) number K935157. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES?

ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES is a medical device that received FDA 510(k) clearance on 1994-08-09. The listed applicant is Regulatory Consultants TO the Medical Device Indus. The 510(k) number is K935157.

When did ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES receive FDA 510(k) clearance?

ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES received FDA 510(k) clearance on 1994-08-09, under 510(k) number K935157.

Who is the listed applicant for ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES?

The FDA 510(k) record lists Regulatory Consultants TO the Medical Device Indus as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES?

The FDA product code for ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES is KPX.

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: KPX)

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.

↑