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)

GRASPING FORCEPS

K-Number: K933261 · 1994-01-11

ApplicantSurgitek
Decision Date1994-01-11
Product CodeFGO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Surgitek. It received FDA 510(k) clearance on 1994-01-11 under 510(k) number K933261. The device is classified under product code FGO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASPING FORCEPS?

GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is Surgitek. The 510(k) number is K933261.

When did GRASPING FORCEPS receive FDA 510(k) clearance?

GRASPING FORCEPS received FDA 510(k) clearance on 1994-01-11, under 510(k) number K933261.

Who is the listed applicant for GRASPING FORCEPS?

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

What is the FDA product code for GRASPING FORCEPS?

The FDA product code for GRASPING FORCEPS is FGO.

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 Surgitek 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 29 devices →

Related Devices (Code: FGO)

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.

↑