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FDA 510(k)

8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO

K-Number: K792196 · 1979-11-13

ApplicantPhotovolt Corp.
Decision Date1979-11-13
Product CodeJJR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO is the device name listed in this FDA 510(k) record. The listed applicant is Photovolt Corp.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792196. The device is classified under product code JJR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO?

8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Photovolt Corp.. The 510(k) number is K792196.

When did 8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO receive FDA 510(k) clearance?

8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792196.

Who is the listed applicant for 8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO?

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

What is the FDA product code for 8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO?

The FDA product code for 8 SUBJECT PHOTOVOLT ELECTROLYTE SERUM CO is JJR.

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 Photovolt 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.

K800453PHOTOVOLT PVA 4M+2 ANALYZER

Related Devices (Code: JJR)

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.

K990971EASYLYTE QUALITY CONTROL KIT, MODELS 2814, 2815, 2816Medica Corp.K960592ELECTROLYTE STANDARDSPhoenix Diagnostics, Inc.K955630RNA MEDICAL HEMAT CONTROLBionostics, Inc.K951435AALTO SCIENTIFIC SWEAT CHLORIDE REFERENCE MATERIALAalto Scientific, Ltd.K943925SWEAT CONTROLS FOR CYSTIC FIBROSIS TESTINGQuantimetrix Corp.K934641I-STAT CONTROL LEVELS 1,2,3I-Stat Corp.

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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