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FDA 510(k)

TEMP. CARDIAC PACING WIRE TME 60/61/65

K-Number: K831695 · 1983-10-20

ApplicantOscor, Inc.
Decision Date1983-10-20
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TEMP. CARDIAC PACING WIRE TME 60/61/65 is the device name listed in this FDA 510(k) record. The listed applicant is Oscor, Inc.. It received FDA 510(k) clearance on 1983-10-20 under 510(k) number K831695. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP. CARDIAC PACING WIRE TME 60/61/65?

TEMP. CARDIAC PACING WIRE TME 60/61/65 is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Oscor, Inc.. The 510(k) number is K831695.

When did TEMP. CARDIAC PACING WIRE TME 60/61/65 receive FDA 510(k) clearance?

TEMP. CARDIAC PACING WIRE TME 60/61/65 received FDA 510(k) clearance on 1983-10-20, under 510(k) number K831695.

Who is the listed applicant for TEMP. CARDIAC PACING WIRE TME 60/61/65?

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

What is the FDA product code for TEMP. CARDIAC PACING WIRE TME 60/61/65?

The FDA product code for TEMP. CARDIAC PACING WIRE TME 60/61/65 is LDF.

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 Oscor, 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 43 devices →

Related Devices (Code: LDF)

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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