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FDA 510(k)

AC-22 AUTOCLAVE TAPE

K-Number: K831722 · 1983-07-06

ApplicantArmak Tape Division
Decision Date1983-07-06
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AC-22 AUTOCLAVE TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Armak Tape Division. It received FDA 510(k) clearance on 1983-07-06 under 510(k) number K831722. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AC-22 AUTOCLAVE TAPE?

AC-22 AUTOCLAVE TAPE is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Armak Tape Division. The 510(k) number is K831722.

When did AC-22 AUTOCLAVE TAPE receive FDA 510(k) clearance?

AC-22 AUTOCLAVE TAPE received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831722.

Who is the listed applicant for AC-22 AUTOCLAVE TAPE?

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

What is the FDA product code for AC-22 AUTOCLAVE TAPE?

The FDA product code for AC-22 AUTOCLAVE TAPE is JOJ.

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Related Devices (Code: JOJ)

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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