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)

LAPAROSCOPIC SUCTION/IRRIGATION PROBE

K-Number: K920643 · 1992-05-06

Decision Date1992-05-06
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC SUCTION/IRRIGATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Concepts, Inc.. It received FDA 510(k) clearance on 1992-05-06 under 510(k) number K920643. The device is classified under product code GBZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC SUCTION/IRRIGATION PROBE?

LAPAROSCOPIC SUCTION/IRRIGATION PROBE is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K920643.

When did LAPAROSCOPIC SUCTION/IRRIGATION PROBE receive FDA 510(k) clearance?

LAPAROSCOPIC SUCTION/IRRIGATION PROBE received FDA 510(k) clearance on 1992-05-06, under 510(k) number K920643.

Who is the listed applicant for LAPAROSCOPIC SUCTION/IRRIGATION PROBE?

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

What is the FDA product code for LAPAROSCOPIC SUCTION/IRRIGATION PROBE?

The FDA product code for LAPAROSCOPIC SUCTION/IRRIGATION PROBE is GBZ.

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 O.R. Concepts, 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 34 devices →

Related Devices (Code: GBZ)

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.

↑