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FDA 510(k)

HOSPITAL KIT SV 105

K-Number: K922133 · 1993-06-07

Decision Date1993-06-07
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

HOSPITAL KIT SV 105 is the device name listed in this FDA 510(k) record. The listed applicant is Savoy Medical Supply Co., Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K922133. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HOSPITAL KIT SV 105?

HOSPITAL KIT SV 105 is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Savoy Medical Supply Co., Inc.. The 510(k) number is K922133.

When did HOSPITAL KIT SV 105 receive FDA 510(k) clearance?

HOSPITAL KIT SV 105 received FDA 510(k) clearance on 1993-06-07, under 510(k) number K922133.

Who is the listed applicant for HOSPITAL KIT SV 105?

The FDA 510(k) record lists Savoy Medical Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOSPITAL KIT SV 105?

The FDA product code for HOSPITAL KIT SV 105 is LRO.

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 Savoy Medical Supply Co., Inc. 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 7 devices →

Related Devices (Code: LRO)

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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