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FDA 510(k)

ANTI-DISCONNECTION MECHANISM

K-Number: K933781 · 1993-09-22

ApplicantHammer-Plane, Inc.
Decision Date1993-09-22
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANTI-DISCONNECTION MECHANISM is the device name listed in this FDA 510(k) record. The listed applicant is Hammer-Plane, Inc.. It received FDA 510(k) clearance on 1993-09-22 under 510(k) number K933781. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-DISCONNECTION MECHANISM?

ANTI-DISCONNECTION MECHANISM is a medical device that received FDA 510(k) clearance on 1993-09-22. The listed applicant is Hammer-Plane, Inc.. The 510(k) number is K933781.

When did ANTI-DISCONNECTION MECHANISM receive FDA 510(k) clearance?

ANTI-DISCONNECTION MECHANISM received FDA 510(k) clearance on 1993-09-22, under 510(k) number K933781.

Who is the listed applicant for ANTI-DISCONNECTION MECHANISM?

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

What is the FDA product code for ANTI-DISCONNECTION MECHANISM?

The FDA product code for ANTI-DISCONNECTION MECHANISM is CBH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Hammer-Plane, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K950098NEEDLE SAFETY COVER

Related Devices (Code: CBH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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