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FDA 510(k)

PG-NUMERIC(TM)

K-Number: K883411 · 1989-03-15

ApplicantIsolab, Inc.
Decision Date1989-03-15
Product CodeJHF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PG-NUMERIC(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Isolab, Inc.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K883411. The device is classified under product code JHF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PG-NUMERIC(TM)?

PG-NUMERIC(TM) is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Isolab, Inc.. The 510(k) number is K883411.

When did PG-NUMERIC(TM) receive FDA 510(k) clearance?

PG-NUMERIC(TM) received FDA 510(k) clearance on 1989-03-15, under 510(k) number K883411.

Who is the listed applicant for PG-NUMERIC(TM)?

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

What is the FDA product code for PG-NUMERIC(TM)?

The FDA product code for PG-NUMERIC(TM) is JHF.

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Other records listing Isolab, Inc. as applicant

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Related Devices (Code: JHF)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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