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FDA 510(k)

BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR

K-Number: K953410 · 1995-09-29

Decision Date1995-09-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Springfield Surgical Instruments. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K953410. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR?

BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Springfield Surgical Instruments. The 510(k) number is K953410.

When did BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR receive FDA 510(k) clearance?

BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR received FDA 510(k) clearance on 1995-09-29, under 510(k) number K953410.

Who is the listed applicant for BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR?

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

What is the FDA product code for BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR?

The FDA product code for BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR is GCJ.

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 Springfield Surgical Instruments 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 →

Related Devices (Code: GCJ)

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.

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