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FDA 510(k)

LITHOTOMY CHAIR #415

K-Number: K831385 · 1983-06-02

ApplicantMidmark Corp.
Decision Date1983-06-02
Product CodeGBB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LITHOTOMY CHAIR #415 is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K831385. The device is classified under product code GBB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHOTOMY CHAIR #415?

LITHOTOMY CHAIR #415 is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Midmark Corp.. The 510(k) number is K831385.

When did LITHOTOMY CHAIR #415 receive FDA 510(k) clearance?

LITHOTOMY CHAIR #415 received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831385.

Who is the listed applicant for LITHOTOMY CHAIR #415?

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

What is the FDA product code for LITHOTOMY CHAIR #415?

The FDA product code for LITHOTOMY CHAIR #415 is GBB.

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 Midmark Corp. 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 31 devices →

Related Devices (Code: GBB)

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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