FDA 510(k)

ALL-BOND(R) JR.

K-Number: K932379 · 1993-07-22

Decision Date1993-07-22

Product CodeKLE

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

ALL-BOND(R) JR. is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932379. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALL-BOND(R) JR.?

ALL-BOND(R) JR. is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Bisco, Inc.. The 510(k) number is K932379.

When did ALL-BOND(R) JR. receive FDA 510(k) clearance?

ALL-BOND(R) JR. received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932379.

Who is the listed applicant for ALL-BOND(R) JR.?

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

What is the FDA product code for ALL-BOND(R) JR.?

The FDA product code for ALL-BOND(R) JR. is KLE.

Other records listing Bisco, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.