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FDA 510(k)

CARAGLAS XTRA SYNTHETIC CASTING TAPE

K-Number: K896634 · 1990-06-14

ApplicantBuckman Co., Inc.
Decision Date1990-06-14
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CARAGLAS XTRA SYNTHETIC CASTING TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1990-06-14 under 510(k) number K896634. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAGLAS XTRA SYNTHETIC CASTING TAPE?

CARAGLAS XTRA SYNTHETIC CASTING TAPE is a medical device that received FDA 510(k) clearance on 1990-06-14. The listed applicant is Buckman Co., Inc.. The 510(k) number is K896634.

When did CARAGLAS XTRA SYNTHETIC CASTING TAPE receive FDA 510(k) clearance?

CARAGLAS XTRA SYNTHETIC CASTING TAPE received FDA 510(k) clearance on 1990-06-14, under 510(k) number K896634.

Who is the listed applicant for CARAGLAS XTRA SYNTHETIC CASTING TAPE?

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

What is the FDA product code for CARAGLAS XTRA SYNTHETIC CASTING TAPE?

The FDA product code for CARAGLAS XTRA SYNTHETIC CASTING TAPE is LGF.

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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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