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FDA 510(k)

LINDEN STONE EXTRACTION BALLOON

K-Number: K872509 · 1987-09-22

ApplicantHobbs Medical, Inc.
Decision Date1987-09-22
Product CodeFGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LINDEN STONE EXTRACTION BALLOON is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 1987-09-22 under 510(k) number K872509. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINDEN STONE EXTRACTION BALLOON?

LINDEN STONE EXTRACTION BALLOON is a medical device that received FDA 510(k) clearance on 1987-09-22. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K872509.

When did LINDEN STONE EXTRACTION BALLOON receive FDA 510(k) clearance?

LINDEN STONE EXTRACTION BALLOON received FDA 510(k) clearance on 1987-09-22, under 510(k) number K872509.

Who is the listed applicant for LINDEN STONE EXTRACTION BALLOON?

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

What is the FDA product code for LINDEN STONE EXTRACTION BALLOON?

The FDA product code for LINDEN STONE EXTRACTION BALLOON is FGE.

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Other records listing Hobbs Medical, Inc. as applicant

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Related Devices (Code: FGE)

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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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