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FDA 510(k)

STERILE WATER 4OZ.

K-Number: K812312 · 1981-11-13

Decision Date1981-11-13
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE WATER 4OZ. is the device name listed in this FDA 510(k) record. The listed applicant is Superior Plastic Products Corp.. It received FDA 510(k) clearance on 1981-11-13 under 510(k) number K812312. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE WATER 4OZ.?

STERILE WATER 4OZ. is a medical device that received FDA 510(k) clearance on 1981-11-13. The listed applicant is Superior Plastic Products Corp.. The 510(k) number is K812312.

When did STERILE WATER 4OZ. receive FDA 510(k) clearance?

STERILE WATER 4OZ. received FDA 510(k) clearance on 1981-11-13, under 510(k) number K812312.

Who is the listed applicant for STERILE WATER 4OZ.?

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

What is the FDA product code for STERILE WATER 4OZ.?

The FDA product code for STERILE WATER 4OZ. is JOL.

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 Superior Plastic Products 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.

View all 15 devices →

Related Devices (Code: JOL)

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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