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FDA 510(k)

SUPRA SCOPE

K-Number: K801050 · 1980-05-14

ApplicantWarner-Lambert Co.
Decision Date1980-05-14
Product CodeBZS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUPRA SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K801050. The device is classified under product code BZS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPRA SCOPE?

SUPRA SCOPE is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Warner-Lambert Co.. The 510(k) number is K801050.

When did SUPRA SCOPE receive FDA 510(k) clearance?

SUPRA SCOPE received FDA 510(k) clearance on 1980-05-14, under 510(k) number K801050.

Who is the listed applicant for SUPRA SCOPE?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPRA SCOPE?

The FDA product code for SUPRA SCOPE is BZS.

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Other records listing Warner-Lambert Co. 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.

K024160NEOSPORIN SCAR SOLUTIONK893452EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAMK870584O.P.T.(TM) OVULATION PREDICTION TESTK861510MULTILUMEN VIAPIC CENTRAL LINE CATHETERK852967GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISKK852689GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK

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Related Devices (Code: BZS)

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.

K935146DISPOSABLE STETHOSCOPE HEAD COVERModern Medical Devices, Inc.K930118STETSKINSNova Diversified Concepts

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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