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FDA 510(k)

ZINDRICK IM ROD

K-Number: K871539 · 1987-08-17

ApplicantBuckman Co., Inc.
Decision Date1987-08-17
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZINDRICK IM ROD 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 1987-08-17 under 510(k) number K871539. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZINDRICK IM ROD?

ZINDRICK IM ROD is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Buckman Co., Inc.. The 510(k) number is K871539.

When did ZINDRICK IM ROD receive FDA 510(k) clearance?

ZINDRICK IM ROD received FDA 510(k) clearance on 1987-08-17, under 510(k) number K871539.

Who is the listed applicant for ZINDRICK IM ROD?

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 ZINDRICK IM ROD?

The FDA product code for ZINDRICK IM ROD is HSB.

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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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