Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

A CALIPER

K-Number: K820659 · 1982-03-19

ApplicantTwin City Surgical, Inc.
Decision Date1982-03-19
Product CodeKTZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A CALIPER 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 1982-03-19 under 510(k) number K820659. The device is classified under product code KTZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A CALIPER?

A CALIPER is a medical device that received FDA 510(k) clearance on 1982-03-19. The listed applicant is Twin City Surgical, Inc.. The 510(k) number is K820659.

When did A CALIPER receive FDA 510(k) clearance?

A CALIPER received FDA 510(k) clearance on 1982-03-19, under 510(k) number K820659.

Who is the listed applicant for A CALIPER?

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 A CALIPER?

The FDA product code for A CALIPER is KTZ.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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) TESTERK861632SIMS CHAIRK830585ANVIL RETRACTORK820660A HOOK DRIVERK813067SPINAL WRENCH

Related Devices (Code: KTZ)

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.

K921266NK MEDICAL MICROMETER, MODEL MC001Nk Biotechnical Engineering Co.K841687SKYNDEX ELECTRONIC BODY FAT CALCULACaldwell, Justiss & Co., Inc.K831898SCOLIMETERDr. Micheal A. SabiaK810116ISOROBIC SKINFOLD CALIPERFitness Motivation Institute of AmericaK800363PARKE-DAVIS TOTAL KNEE PROSTHESISWarner-Lambert Co.K760521TAPE MEASUREMcgaw Laboratories

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.

↑