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FDA 510(k)

LIC TILT BED

K-Number: K830633 · 1983-03-10

Decision Date1983-03-10
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIC TILT BED is the device name listed in this FDA 510(k) record. The listed applicant is Century Manufacturing Co.. It received FDA 510(k) clearance on 1983-03-10 under 510(k) number K830633. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIC TILT BED?

LIC TILT BED is a medical device that received FDA 510(k) clearance on 1983-03-10. The listed applicant is Century Manufacturing Co.. The 510(k) number is K830633.

When did LIC TILT BED receive FDA 510(k) clearance?

LIC TILT BED received FDA 510(k) clearance on 1983-03-10, under 510(k) number K830633.

Who is the listed applicant for LIC TILT BED?

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

What is the FDA product code for LIC TILT BED?

The FDA product code for LIC TILT BED is INQ.

Other records listing Century Manufacturing 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 12 devices →

Related Devices (Code: INQ)

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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