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FDA 510(k)

VERSCHLUBSTOPFEN COMB-CLOSING STOPPER

K-Number: K813396 · 1982-01-12

Decision Date1982-01-12
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERSCHLUBSTOPFEN COMB-CLOSING STOPPER is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1982-01-12 under 510(k) number K813396. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSCHLUBSTOPFEN COMB-CLOSING STOPPER?

VERSCHLUBSTOPFEN COMB-CLOSING STOPPER is a medical device that received FDA 510(k) clearance on 1982-01-12. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K813396.

When did VERSCHLUBSTOPFEN COMB-CLOSING STOPPER receive FDA 510(k) clearance?

VERSCHLUBSTOPFEN COMB-CLOSING STOPPER received FDA 510(k) clearance on 1982-01-12, under 510(k) number K813396.

Who is the listed applicant for VERSCHLUBSTOPFEN COMB-CLOSING STOPPER?

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

What is the FDA product code for VERSCHLUBSTOPFEN COMB-CLOSING STOPPER?

The FDA product code for VERSCHLUBSTOPFEN COMB-CLOSING STOPPER is FOZ.

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 Burron Medical Products, Inc. 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 41 devices →

Related Devices (Code: FOZ)

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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