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FDA 510(k)

SILOAM SAVE-A-NEEDLE

K-Number: K820502 · 1982-03-15

ApplicantSiloam, Inc.
Decision Date1982-03-15
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILOAM SAVE-A-NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Siloam, Inc.. It received FDA 510(k) clearance on 1982-03-15 under 510(k) number K820502. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILOAM SAVE-A-NEEDLE?

SILOAM SAVE-A-NEEDLE is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Siloam, Inc.. The 510(k) number is K820502.

When did SILOAM SAVE-A-NEEDLE receive FDA 510(k) clearance?

SILOAM SAVE-A-NEEDLE received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820502.

Who is the listed applicant for SILOAM SAVE-A-NEEDLE?

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

What is the FDA product code for SILOAM SAVE-A-NEEDLE?

The FDA product code for SILOAM SAVE-A-NEEDLE is GAA.

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Related Devices (Code: GAA)

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.

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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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