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FDA 510(k)

ACE PNEUMATIC OSCILLATING SAW

K-Number: K881250 · 1988-04-15

ApplicantBuckman Co., Inc.
Decision Date1988-04-15
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACE PNEUMATIC OSCILLATING SAW 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 1988-04-15 under 510(k) number K881250. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE PNEUMATIC OSCILLATING SAW?

ACE PNEUMATIC OSCILLATING SAW is a medical device that received FDA 510(k) clearance on 1988-04-15. The listed applicant is Buckman Co., Inc.. The 510(k) number is K881250.

When did ACE PNEUMATIC OSCILLATING SAW receive FDA 510(k) clearance?

ACE PNEUMATIC OSCILLATING SAW received FDA 510(k) clearance on 1988-04-15, under 510(k) number K881250.

Who is the listed applicant for ACE PNEUMATIC OSCILLATING SAW?

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 ACE PNEUMATIC OSCILLATING SAW?

The FDA product code for ACE PNEUMATIC OSCILLATING SAW is HSZ.

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Related Devices (Code: HSZ)

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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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