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FDA 510(k)

LEININGEO AORTIC PUNCH #310-395 & 397

K-Number: K771625 · 1977-09-12

ApplicantJ. Jamner Surgical Instruments, Inc.
Decision Date1977-09-12
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEININGEO AORTIC PUNCH #310-395 & 397 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 1977-09-12 under 510(k) number K771625. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEININGEO AORTIC PUNCH #310-395 & 397?

LEININGEO AORTIC PUNCH #310-395 & 397 is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is J. Jamner Surgical Instruments, Inc.. The 510(k) number is K771625.

When did LEININGEO AORTIC PUNCH #310-395 & 397 receive FDA 510(k) clearance?

LEININGEO AORTIC PUNCH #310-395 & 397 received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771625.

Who is the listed applicant for LEININGEO AORTIC PUNCH #310-395 & 397?

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 LEININGEO AORTIC PUNCH #310-395 & 397?

The FDA product code for LEININGEO AORTIC PUNCH #310-395 & 397 is DWS.

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Other records listing J. Jamner Surgical Instruments, Inc. as applicant

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Related Devices (Code: DWS)

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.

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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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