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FDA 510(k)

VASPAR SEALANT

K-Number: K792702 · 1980-01-24

ApplicantMeridian Diagnostics, Inc.
Decision Date1980-01-24
Product CodeKEQ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

VASPAR SEALANT is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-24 under 510(k) number K792702. The device is classified under product code KEQ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASPAR SEALANT?

VASPAR SEALANT is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K792702.

When did VASPAR SEALANT receive FDA 510(k) clearance?

VASPAR SEALANT received FDA 510(k) clearance on 1980-01-24, under 510(k) number K792702.

Who is the listed applicant for VASPAR SEALANT?

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

What is the FDA product code for VASPAR SEALANT?

The FDA product code for VASPAR SEALANT is KEQ.

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Other records listing Meridian Diagnostics, 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.

K993914PREMIER TOXINS A&B, MODEL 616096K990263IMMUNOCARD STAT! E. COLI O157:H7K984343PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TESTK984346PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TESTK983255MODIFICATION TO: PREMIER PLATINUM HPSAK982764PREMIER CRYPTOSPORIDIUM

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Related Devices (Code: KEQ)

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.

K830515SCOTTS TAP WATER SUBSTITUTE CONCENTRATESurgipath Medical Industries, Inc.K792703LACTO-PHENOL ANALINE BLUE FLUIDMeridian Diagnostics, Inc.K792709KOH MOUNTING FLUID W/GLYCEROLMeridian Diagnostics, Inc.K781868DROPPER, CEPTI-SEAL LAVTOPHENOLMarion Laboratories, Inc.K781869DROPPER, CEPTI-SEAL KOH SOLUTIONMarion Laboratories, Inc.K781388F.A. MOUNTING MEDIUMFlow Laboratories, Inc.

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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