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FDA 510(k)

SCANNING SYS., AUTO. COMP., ACS1000

K-Number: K772140 · 1977-12-05

ApplicantHoneywell, Inc.
Decision Date1977-12-05
Product CodeJOY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SCANNING SYS., AUTO. COMP., ACS1000 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1977-12-05 under 510(k) number K772140. The device is classified under product code JOY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANNING SYS., AUTO. COMP., ACS1000?

SCANNING SYS., AUTO. COMP., ACS1000 is a medical device that received FDA 510(k) clearance on 1977-12-05. The listed applicant is Honeywell, Inc.. The 510(k) number is K772140.

When did SCANNING SYS., AUTO. COMP., ACS1000 receive FDA 510(k) clearance?

SCANNING SYS., AUTO. COMP., ACS1000 received FDA 510(k) clearance on 1977-12-05, under 510(k) number K772140.

Who is the listed applicant for SCANNING SYS., AUTO. COMP., ACS1000?

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 SCANNING SYS., AUTO. COMP., ACS1000?

The FDA product code for SCANNING SYS., AUTO. COMP., ACS1000 is JOY.

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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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