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FDA 510(k)

BACH-SIMPSON MODEL TS266

K-Number: K811616 · 1981-08-13

Decision Date1981-08-13
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BACH-SIMPSON MODEL TS266 is the device name listed in this FDA 510(k) record. The listed applicant is Bach-Simpson , Ltd.. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K811616. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACH-SIMPSON MODEL TS266?

BACH-SIMPSON MODEL TS266 is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Bach-Simpson , Ltd.. The 510(k) number is K811616.

When did BACH-SIMPSON MODEL TS266 receive FDA 510(k) clearance?

BACH-SIMPSON MODEL TS266 received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811616.

Who is the listed applicant for BACH-SIMPSON MODEL TS266?

The FDA 510(k) record lists Bach-Simpson , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACH-SIMPSON MODEL TS266?

The FDA product code for BACH-SIMPSON MODEL TS266 is DPW.

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 Bach-Simpson , Ltd. 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.

Related Devices (Code: DPW)

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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