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FDA 510(k)

IONOMETER EF AND ACCESSORIES

K-Number: K870183 · 1987-05-12

ApplicantSmash Ent., Inc.
Decision Date1987-05-12
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IONOMETER EF AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Smash Ent., Inc.. It received FDA 510(k) clearance on 1987-05-12 under 510(k) number K870183. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONOMETER EF AND ACCESSORIES?

IONOMETER EF AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1987-05-12. The listed applicant is Smash Ent., Inc.. The 510(k) number is K870183.

When did IONOMETER EF AND ACCESSORIES receive FDA 510(k) clearance?

IONOMETER EF AND ACCESSORIES received FDA 510(k) clearance on 1987-05-12, under 510(k) number K870183.

Who is the listed applicant for IONOMETER EF AND ACCESSORIES?

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

What is the FDA product code for IONOMETER EF AND ACCESSORIES?

The FDA product code for IONOMETER EF AND ACCESSORIES is JGS.

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.

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Other records listing Smash Ent., Inc. 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.

K880857SYRINGE PUMP MS2000K881162ENTERA* ENTERAL FEEDING BAGK880373IONOMETER E-HK AND ACCESSORIES

Related Devices (Code: JGS)

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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