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FDA 510(k)

EXTENSION BOX EB200

K-Number: K834530 · 1984-06-01

ApplicantHoneywell, Inc.
Decision Date1984-06-01
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EXTENSION BOX EB200 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K834530. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION BOX EB200?

EXTENSION BOX EB200 is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Honeywell, Inc.. The 510(k) number is K834530.

When did EXTENSION BOX EB200 receive FDA 510(k) clearance?

EXTENSION BOX EB200 received FDA 510(k) clearance on 1984-06-01, under 510(k) number K834530.

Who is the listed applicant for EXTENSION BOX EB200?

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

What is the FDA product code for EXTENSION BOX EB200?

The FDA product code for EXTENSION BOX EB200 is DRT.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DRT)

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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