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FDA 510(k)

COVERAGE SPRAY HBV

K-Number: K964835 · 1996-12-16

Decision Date1996-12-16
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COVERAGE SPRAY HBV is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1996-12-16 under 510(k) number K964835. The device is classified under product code LRJ. It was reviewed by the HO advisory panel. Product code LRJ falls under the category of Clinical Lab, which includes general clinical laboratory instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COVERAGE SPRAY HBV?

COVERAGE SPRAY HBV is a medical device that received FDA 510(k) clearance on 1996-12-16. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K964835.

When did COVERAGE SPRAY HBV receive FDA 510(k) clearance?

COVERAGE SPRAY HBV received FDA 510(k) clearance on 1996-12-16, under 510(k) number K964835.

Who is the listed applicant for COVERAGE SPRAY HBV?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COVERAGE SPRAY HBV?

The FDA product code for COVERAGE SPRAY HBV is LRJ. This falls under the Clinical Lab category.

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 Convatec, A Division of E.R. Squibb & Sons 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 81 devices →

Related Devices (Code: LRJ)

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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