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FDA 510(k)

OSMOMETER STANDARD SOLUTIONS

K-Number: K892329 · 1989-10-31

ApplicantD.R.G. Scientific Industries
Decision Date1989-10-31
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OSMOMETER STANDARD SOLUTIONS is the device name listed in this FDA 510(k) record. The listed applicant is D.R.G. Scientific Industries. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K892329. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSMOMETER STANDARD SOLUTIONS?

OSMOMETER STANDARD SOLUTIONS is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is D.R.G. Scientific Industries. The 510(k) number is K892329.

When did OSMOMETER STANDARD SOLUTIONS receive FDA 510(k) clearance?

OSMOMETER STANDARD SOLUTIONS received FDA 510(k) clearance on 1989-10-31, under 510(k) number K892329.

Who is the listed applicant for OSMOMETER STANDARD SOLUTIONS?

The FDA 510(k) record lists D.R.G. Scientific Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSMOMETER STANDARD SOLUTIONS?

The FDA product code for OSMOMETER STANDARD SOLUTIONS is JIT.

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Other records listing D.R.G. Scientific Industries 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.

K870889ACID FUCHSIN SOLUTIONSK863880BLOOD GASES/ PO2, PCO2 AND BLOOD PH ANALYSIS PROD.K863825CO-OXIMETER SOLUTIONSK863824SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.

Related Devices (Code: JIT)

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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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