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FDA 510(k)

ASTRA PRINTER PAPER #88112-CHLORIDE SILV

K-Number: K802392 · 1980-10-23

ApplicantHi Chem, Inc.
Decision Date1980-10-23
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ASTRA PRINTER PAPER #88112-CHLORIDE SILV is the device name listed in this FDA 510(k) record. The listed applicant is Hi Chem, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802392. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTRA PRINTER PAPER #88112-CHLORIDE SILV?

ASTRA PRINTER PAPER #88112-CHLORIDE SILV is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Hi Chem, Inc.. The 510(k) number is K802392.

When did ASTRA PRINTER PAPER #88112-CHLORIDE SILV receive FDA 510(k) clearance?

ASTRA PRINTER PAPER #88112-CHLORIDE SILV received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802392.

Who is the listed applicant for ASTRA PRINTER PAPER #88112-CHLORIDE SILV?

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

What is the FDA product code for ASTRA PRINTER PAPER #88112-CHLORIDE SILV?

The FDA product code for ASTRA PRINTER PAPER #88112-CHLORIDE SILV is JJF.

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 Hi Chem, 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.

View all 52 devices →

Related Devices (Code: JJF)

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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