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FDA 510(k)

DISPOSABLE TAIYANG SYRINGE

K-Number: K822238 · 1982-08-25

ApplicantS.D. Sunnyland Enterprises, Inc.
Decision Date1982-08-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE TAIYANG SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is S.D. Sunnyland Enterprises, Inc.. It received FDA 510(k) clearance on 1982-08-25 under 510(k) number K822238. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE TAIYANG SYRINGE?

DISPOSABLE TAIYANG SYRINGE is a medical device that received FDA 510(k) clearance on 1982-08-25. The listed applicant is S.D. Sunnyland Enterprises, Inc.. The 510(k) number is K822238.

When did DISPOSABLE TAIYANG SYRINGE receive FDA 510(k) clearance?

DISPOSABLE TAIYANG SYRINGE received FDA 510(k) clearance on 1982-08-25, under 510(k) number K822238.

Who is the listed applicant for DISPOSABLE TAIYANG SYRINGE?

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

What is the FDA product code for DISPOSABLE TAIYANG SYRINGE?

The FDA product code for DISPOSABLE TAIYANG SYRINGE is FMF.

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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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