FDA 510(k)

UNKNOWN

K-Number: K837283 · 1983-04-15

Decision Date1983-04-15

Product Code

DecisionSubstantially Equivalent

Device Summary

UNKNOWN is the device name listed in this FDA 510(k) record. The listed applicant is Tannhut. It received FDA 510(k) clearance on 1983-04-15 under 510(k) number K837283. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNKNOWN?

UNKNOWN is a medical device that received FDA 510(k) clearance on 1983-04-15. The listed applicant is Tannhut. The 510(k) number is K837283.

When did UNKNOWN receive FDA 510(k) clearance?

UNKNOWN received FDA 510(k) clearance on 1983-04-15, under 510(k) number K837283.

Who is the listed applicant for UNKNOWN?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Tannhut as applicant

K851858FOLD AWAY HUT K851859FACIAL/UPPER BODY UNIT K851255SUN BEDS K840137SILGMANN SOLARIUM S-TYPE 1218 COMBO K812579SUNTANNING HOME UNIT K802756SEMI-OVAL MODULAR SUNTANNING BOOTH

View all 7 devices →

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.