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FDA 510(k)

S.S.C. MEDICAL MODEL 5000 SERIES BED

K-Number: K934090 · 1994-02-09

Decision Date1994-02-09
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

S.S.C. MEDICAL MODEL 5000 SERIES BED is the device name listed in this FDA 510(k) record. The listed applicant is Super Sagless Corp.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K934090. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S.S.C. MEDICAL MODEL 5000 SERIES BED?

S.S.C. MEDICAL MODEL 5000 SERIES BED is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Super Sagless Corp.. The 510(k) number is K934090.

When did S.S.C. MEDICAL MODEL 5000 SERIES BED receive FDA 510(k) clearance?

S.S.C. MEDICAL MODEL 5000 SERIES BED received FDA 510(k) clearance on 1994-02-09, under 510(k) number K934090.

Who is the listed applicant for S.S.C. MEDICAL MODEL 5000 SERIES BED?

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

What is the FDA product code for S.S.C. MEDICAL MODEL 5000 SERIES BED?

The FDA product code for S.S.C. MEDICAL MODEL 5000 SERIES BED is FNL.

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 Super Sagless 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.

Related Devices (Code: FNL)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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