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FDA 510(k)

SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC)

K-Number: K864414 · 1986-12-18

Decision Date1986-12-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC) is the device name listed in this FDA 510(k) record. The listed applicant is Seal Syringe Corp.. It received FDA 510(k) clearance on 1986-12-18 under 510(k) number K864414. 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 SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC)?

SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC) is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Seal Syringe Corp.. The 510(k) number is K864414.

When did SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC) receive FDA 510(k) clearance?

SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC) received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864414.

Who is the listed applicant for SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC)?

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

What is the FDA product code for SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC)?

The FDA product code for SEAL SYRINGE (3CC,5CC,12CC,20CC,30CC & 50CC) is FMF.

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.

Related Devices (Code: FMF)

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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