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FDA 510(k)

THE (CROM) TESTER

K-Number: K870767 · 1987-03-17

ApplicantTwin City Surgical, Inc.
Decision Date1987-03-17
Product CodeKQW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE (CROM) TESTER 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 1987-03-17 under 510(k) number K870767. The device is classified under product code KQW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE (CROM) TESTER?

THE (CROM) TESTER is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Twin City Surgical, Inc.. The 510(k) number is K870767.

When did THE (CROM) TESTER receive FDA 510(k) clearance?

THE (CROM) TESTER received FDA 510(k) clearance on 1987-03-17, under 510(k) number K870767.

Who is the listed applicant for THE (CROM) TESTER?

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 THE (CROM) TESTER?

The FDA product code for THE (CROM) TESTER is KQW.

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.

K861632SIMS CHAIRK830585ANVIL RETRACTORK820659A CALIPERK820660A HOOK DRIVERK813067SPINAL WRENCH

Related Devices (Code: KQW)

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.

K926237O'BRIEN GONIOMETERSgarlato Laboratories, Inc.K901744DOBBHOFF(R) RETRIEVAL FORCEPSBiosearch Medical Products, Inc.K850082HAND HELD GONIOMETERChattanooga Group, Inc.K831550FINGER BONIOMETER BK7506Fred Sammons, Inc.K812778THE TELOS EQUIPMENTThe Telos Co.K810441UNIVERSAL GONIMETERFred Sammons, Inc.

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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