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FDA 510(k)

INTERSTIM 100 SYSTEM

K-Number: K861136 · 1986-07-09

ApplicantBuckman Co., Inc.
Decision Date1986-07-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

INTERSTIM 100 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1986-07-09 under 510(k) number K861136. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the INTERSTIM 100 SYSTEM?

INTERSTIM 100 SYSTEM is a medical device that received FDA 510(k) clearance on 1986-07-09. The listed applicant is Buckman Co., Inc.. The 510(k) number is K861136.

When did INTERSTIM 100 SYSTEM receive FDA 510(k) clearance?

INTERSTIM 100 SYSTEM received FDA 510(k) clearance on 1986-07-09, under 510(k) number K861136.

Who is the listed applicant for INTERSTIM 100 SYSTEM?

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

What is the FDA product code for INTERSTIM 100 SYSTEM?

The FDA product code for INTERSTIM 100 SYSTEM is IPF.

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Related Devices (Code: IPF)

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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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