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FDA 510(k)

COPE LUNG FORCEPS #305-218

K-Number: K771624 · 1977-09-06

Decision Date1977-09-06
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COPE LUNG FORCEPS #305-218 is the device name listed in this FDA 510(k) record. The listed applicant is J. Jamner Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1977-09-06 under 510(k) number K771624. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPE LUNG FORCEPS #305-218?

COPE LUNG FORCEPS #305-218 is a medical device that received FDA 510(k) clearance on 1977-09-06. The listed applicant is J. Jamner Surgical Instruments, Inc.. The 510(k) number is K771624.

When did COPE LUNG FORCEPS #305-218 receive FDA 510(k) clearance?

COPE LUNG FORCEPS #305-218 received FDA 510(k) clearance on 1977-09-06, under 510(k) number K771624.

Who is the listed applicant for COPE LUNG FORCEPS #305-218?

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

What is the FDA product code for COPE LUNG FORCEPS #305-218?

The FDA product code for COPE LUNG FORCEPS #305-218 is GEN.

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 J. Jamner Surgical Instruments, 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 11 devices →

Related Devices (Code: GEN)

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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