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FDA 510(k)

ANA TRANS TUBE & SWABS STERILE PACK

K-Number: K834357 · 1984-01-31

Decision Date1984-01-31
Product CodeJSL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANA TRANS TUBE & SWABS STERILE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1984-01-31 under 510(k) number K834357. The device is classified under product code JSL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANA TRANS TUBE & SWABS STERILE PACK?

ANA TRANS TUBE & SWABS STERILE PACK is a medical device that received FDA 510(k) clearance on 1984-01-31. The listed applicant is Anaerobe Systems. The 510(k) number is K834357.

When did ANA TRANS TUBE & SWABS STERILE PACK receive FDA 510(k) clearance?

ANA TRANS TUBE & SWABS STERILE PACK received FDA 510(k) clearance on 1984-01-31, under 510(k) number K834357.

Who is the listed applicant for ANA TRANS TUBE & SWABS STERILE PACK?

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

What is the FDA product code for ANA TRANS TUBE & SWABS STERILE PACK?

The FDA product code for ANA TRANS TUBE & SWABS STERILE PACK is JSL.

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.

Other records listing Anaerobe Systems 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.

View all 52 devices →

Related Devices (Code: JSL)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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