FDA 510(k)

AUTOSECTOR

K-Number: K837499 · 1983-06-10

Decision Date1983-06-10

Product Code

DecisionSubstantially Equivalent

Device Summary

AUTOSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1983-06-10 under 510(k) number K837499. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOSECTOR?

AUTOSECTOR is a medical device that received FDA 510(k) clearance on 1983-06-10. The listed applicant is Technicare Corp.. The 510(k) number is K837499.

When did AUTOSECTOR receive FDA 510(k) clearance?

AUTOSECTOR received FDA 510(k) clearance on 1983-06-10, under 510(k) number K837499.

Who is the listed applicant for AUTOSECTOR?

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

Related Clinical Trials

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Other records listing Technicare Corp. as applicant

K854340TECHNICARE 720 HPS CT SCANNER K852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEM K844293AUTO DII MULTI FREQUENCY K844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS K843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-K842777AUTOFOCUS DUAL ELEMENT PROBE

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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.