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FDA 510(k)

SIMS CHAIR

K-Number: K861632 · 1986-05-27

ApplicantTwin City Surgical, Inc.
Decision Date1986-05-27
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SIMS CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Twin City Surgical, Inc.. It received FDA 510(k) clearance on 1986-05-27 under 510(k) number K861632. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS CHAIR?

SIMS CHAIR is a medical device that received FDA 510(k) clearance on 1986-05-27. The listed applicant is Twin City Surgical, Inc.. The 510(k) number is K861632.

When did SIMS CHAIR receive FDA 510(k) clearance?

SIMS CHAIR received FDA 510(k) clearance on 1986-05-27, under 510(k) number K861632.

Who is the listed applicant for SIMS CHAIR?

The FDA 510(k) record lists Twin City Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMS CHAIR?

The FDA product code for SIMS CHAIR is IKK.

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.

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Other records listing Twin City Surgical, 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.

K870767THE (CROM) TESTERK830585ANVIL RETRACTORK820659A CALIPERK820660A HOOK DRIVERK813067SPINAL WRENCH

Related Devices (Code: IKK)

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.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

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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