FDA 510(k)

SAV-A-LIMB

K-Number: K833872 · 1984-02-04

Decision Date1984-02-04

Product CodeKYR

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SAV-A-LIMB is the device name listed in this FDA 510(k) record. The listed applicant is Sil-Med Corp.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K833872. The device is classified under product code KYR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAV-A-LIMB?

SAV-A-LIMB is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Sil-Med Corp.. The 510(k) number is K833872.

When did SAV-A-LIMB receive FDA 510(k) clearance?

SAV-A-LIMB received FDA 510(k) clearance on 1984-02-04, under 510(k) number K833872.

Who is the listed applicant for SAV-A-LIMB?

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

What is the FDA product code for SAV-A-LIMB?

The FDA product code for SAV-A-LIMB is KYR.

Other records listing Sil-Med 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.

K972521NAVIGATOR (STYLET) 2006 K961392ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II K961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN K961295SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR K960099PENROSE DRAIN MODELS 6001 - 6007 K955463GRIP-A-BOOTS

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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.