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FDA 510(k)

CHAIR, ATTACHED INSTRUMENT DEL. SYS.

K-Number: K760322 · 1976-08-03

Decision Date1976-08-03
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHAIR, ATTACHED INSTRUMENT DEL. SYS. is the device name listed in this FDA 510(k) record. The listed applicant is The S. S. White Co.. It received FDA 510(k) clearance on 1976-08-03 under 510(k) number K760322. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHAIR, ATTACHED INSTRUMENT DEL. SYS.?

CHAIR, ATTACHED INSTRUMENT DEL. SYS. is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is The S. S. White Co.. The 510(k) number is K760322.

When did CHAIR, ATTACHED INSTRUMENT DEL. SYS. receive FDA 510(k) clearance?

CHAIR, ATTACHED INSTRUMENT DEL. SYS. received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760322.

Who is the listed applicant for CHAIR, ATTACHED INSTRUMENT DEL. SYS.?

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

What is the FDA product code for CHAIR, ATTACHED INSTRUMENT DEL. SYS.?

The FDA product code for CHAIR, ATTACHED INSTRUMENT DEL. SYS. is KLC.

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 The S. S. White Co. 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.

View all 14 devices →

Related Devices (Code: KLC)

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

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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